[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100612671":3},{"organization":4,"outcomesModule":7,"designInfo":14,"detailedDescription":25,"studyPopulation":13,"armGroups":26,"interventions":38,"overallOfficials":13,"centralContacts":44,"locations":51,"responsibleParty":66,"collaborators":13,"id":70,"slug":13,"hasResults":71,"nctId":72,"briefTitle":73,"officialTitle":74,"acronym":75,"eligibilityCriteria":76,"healthyVolunteers":71,"sex":77,"minAge":78,"maxAge":79,"enrollmentInfo":80,"targetDuration":13,"studyType":83,"phases":84,"briefSummary":86,"conditions":87,"keywords":91,"overallStatus":54,"whyStopped":13,"lastUpdateSubmitDate":108,"lastUpdatePostDateStruct":109,"startDateStruct":112,"completionDateStruct":114,"leadSponsor":116,"locationsCount":117},{"fullName":5,"class":6},"Dow University of Health Sciences","OTHER",{"primaryOutcomes":8,"secondaryOutcomes":13,"otherOutcomes":13},[9],{"measure":10,"description":11,"timeFrame":12},"Change from Baseline in Serum Creatinine, Blood Urea Nitrogen, and Estimated Glomerular Filtration Rate (eGFR) at 90 Days After Non-Surgical Periodontal Therapy","The primary outcome will be evaluated by measuring changes in renal function biomarkers, including serum creatinine (mg\u002FdL), blood urea nitrogen (BUN, mg\u002FdL), and estimated glomerular filtration rate (eGFR, mL\u002Fmin\u002F1.73 m²). These parameters will be assessed at baseline and 90 days post-intervention to determine within- and between-group differences. Serum creatinine and BUN will be analyzed using standard automated laboratory methods, and eGFR will be calculated using the Modification of Diet in Renal Disease (MDRD) equation. A reduction in serum creatinine and BUN levels and an increase in eGFR will indicate improvement in renal function. Data will be statistically analyzed using Wilcoxon signed-rank and Mann-Whitney U tests with a significance threshold of p ≤ 0.05","Baseline and 90 days after completion of non-surgical periodontal therapy",null,{"allocation":15,"interventionModel":16,"interventionModelDescription":17,"primaryPurpose":18,"observationalModel":13,"timePerspective":13,"maskingInfo":19},"RANDOMIZED","PARALLEL","Parallel Assignment - Participants are randomly assigned to one of two groups: an intervention group receiving non-surgical periodontal therapy and a control group receiving delayed therapy after the study period.","PREVENTION",{"masking":20,"maskingDescription":13,"whoMasked":21},"TRIPLE",[22,23,24],"PARTICIPANT","INVESTIGATOR","OUTCOMES_ASSESSOR","Detailed Description Background and Rationale\n\nPeriodontitis and type 2 diabetes mellitus (T2DM) are both chronic, non-communicable diseases with a well-established bidirectional relationship. Individuals with poorly controlled diabetes are at higher risk of developing periodontal inflammation, while untreated periodontitis may contribute to poor glycemic control through systemic inflammation. Among the microvascular complications of diabetes, nephropathy remains a major cause of morbidity and mortality. It is characterized by glomerular damage, resulting in elevated serum creatinine (SCr) and urea levels, and a reduced glomerular filtration rate (GFR).\n\nAlthough several studies have shown that periodontal therapy can improve glycemic control, there is limited evidence regarding its effects on renal function in diabetic patients. The systemic inflammatory burden caused by chronic periodontitis may exacerbate kidney dysfunction, as inflammatory mediators such as TNF-α, IL-1β, and prostaglandin E2 circulate systemically and contribute to endothelial damage. This study aims to evaluate whether non-surgical periodontal therapy (NSPT), by reducing periodontal inflammation and bacterial load, can positively influence renal biomarkers in patients with uncontrolled type 2 diabetes mellitus.\n\nThe study will provide preliminary interventional data on the potential of periodontal therapy as an adjunctive measure in reducing systemic inflammatory load and possibly delaying microvascular complications, such as diabetic nephropathy. This is particularly relevant in the Pakistani population, where both T2DM and periodontitis have high prevalence, yet local interventional evidence remains scarce.\n\nStudy Design and Setting\n\nThis is a parallel-arm, single-blinded randomized controlled clinical trial designed to evaluate the effect of NSPT on renal function markers in uncontrolled T2DM patients with moderate to severe periodontitis. The study will be conducted at two sites under Dow University of Health Sciences (DUHS), Karachi:\n\nNational Institute of Diabetes and Endocrinology (NIDE) - patient screening and medical evaluation.\n\nDr. Ishrat-ul-Ebad Khan Institute of Oral Health Sciences (DIKIOHS) - periodontal examination and intervention.\n\nThe total duration of the study is projected to be 12 months, including patient recruitment, intervention, 3-month follow-up, data analysis, and report preparation.\n\nSample Size and Allocation\n\nBased on previous studies assessing serum creatinine differences between periodontitis and non-periodontitis groups, a sample size of 23 participants per arm (n=46 total) has been calculated, accounting for 20% attrition. Participants will be randomly assigned to one of two groups using computer-generated random numbers and allocation concealment via Serially Numbered Opaque Sealed Envelopes (SNOSE).\n\nTest Group: Non-surgical periodontal therapy (scaling and root planing) + standardized oral hygiene instructions (OHI).\n\nControl Group: OHI only; scaling and root planing provided after study completion as delayed therapy (DT).\n\nThe principal investigator will remain blinded to the intervention assignment during data collection and analysis.\n\nIntervention Details\n\n1. Non-Surgical Periodontal Therapy (NSPT)\n\n   The NSPT intervention includes full-mouth ultrasonic scaling followed by manual root planing using Gracey curettes. This will be performed in a single session by trained and calibrated dental hygienists under supervision. The procedure aims to remove supra- and sub-gingival plaque and calculus, thereby eliminating bacterial niches contributing to inflammation.\n2. Oral Hygiene Instructions (OHI)\n\n   All participants will receive standardized instructions based on the Modified Stillman's brushing technique using a soft-bristle toothbrush and fluoridated toothpaste twice daily. Each participant will receive an identical oral hygiene kit to ensure standardization. Compliance will be monitored through self-maintained daily practice sheets reviewed at follow-up visits.\n3. Delayed Therapy (DT)\n\nParticipants in the control arm will receive the same NSPT procedure after completion of the 90-day follow-up period to ensure ethical equivalence.\n\nClinical and Laboratory Assessments Baseline Examination\n\nAt recruitment, each participant will undergo:\n\nFull-mouth periodontal charting (six sites per tooth) for probing depth (PPD), clinical attachment loss (CAL), and bleeding on probing (BOP).\n\nCollection of demographic, medical, and lifestyle data via structured questionnaire.\n\nBlood sampling for baseline measurement of:\n\nSerum creatinine (SCr)\n\nBlood urea nitrogen (BUN)\n\nGlycated hemoglobin (HbA1c)\n\nEstimated glomerular filtration rate (eGFR), calculated using the Modification of Diet in Renal Disease (MDRD) formula.\n\nFollow-Up Examination\n\nAt 90 days post-intervention, all parameters will be re-evaluated to assess intra- and inter-group changes in renal and periodontal health indices.\n\nBlood samples will be collected under aseptic conditions by trained personnel and analyzed by the Dow Diagnostic Laboratory using standardized procedures. Serum separation will be done by centrifugation; assays will follow clinical laboratory reference ranges:\n\nSCr normal range: 0.6-1.5 mg\u002FdL\n\nBUN normal range: 30-40 mg\u002FdL\n\nNormal eGFR cutoff: ≥60 mL\u002Fmin\u002F1.73 m²\n\nCalibration and Quality Control\n\nAll periodontal examinations will be performed by the principal investigator (PI), trained and calibrated against a gold standard examiner (the supervisor). Inter- and intra-examiner reliability will be tested before trial initiation using kappa statistics and intra-class correlation coefficients. The two dental hygienists performing the interventions will undergo calibration sessions to standardize SRP procedures. Random 10% re-evaluation of data will be done to ensure consistency.\n\nData Management and Statistical Analysis\n\nAll data will be anonymized using unique participant identifiers. Data entry will be performed using IBM SPSS version 26.0.\n\nContinuous variables will be expressed as mean ± standard deviation, and categorical variables as frequencies and percentages.\n\nStatistical analyses will include:\n\nWilcoxon signed-rank test: for within-group comparisons (baseline vs. 90-day values).\n\nMann-Whitney U test: for between-group comparisons.\n\nCorrelation analyses: between periodontal parameters (PPD, CAL, BOP) and renal markers (SCr, BUN, eGFR).\n\nSignificance level: p ≤ 0.05. Both per-protocol (PPA) and intention-to-treat (ITT) analyses will be performed to ensure robustness of findings.\n\nEthical Considerations\n\nThe study protocol has been reviewed and approved by the Institutional Review Board (IRB) of Dow University of Health Sciences. Written informed consent will be obtained from all participants prior to enrollment, with separate consent forms in English and Urdu to ensure understanding.\n\nParticipation is voluntary, and subjects may withdraw at any stage without penalty. All laboratory and dental procedures will be conducted free of cost. Participants in the control group will receive their complete periodontal therapy after the trial. Data confidentiality will be maintained through de-identification and restricted access.\n\nPotential risks include mild discomfort during blood sampling and transient tooth sensitivity following SRP, both of which are minor and self-limiting. No major adverse effects are anticipated. Participants will have access to dental and medical support throughout the study period.\n\nExpected Outcomes\n\nThe study anticipates a measurable improvement in renal function biomarkers (reduction in SCr and BUN levels, and improvement in eGFR) among the NSPT group compared to controls after 90 days. This would support the hypothesis that periodontal inflammation contributes to systemic inflammatory load affecting renal physiology.\n\nFindings will help strengthen the understanding of oral-systemic health connections and may encourage multidisciplinary management of diabetic patients involving both dental and medical professionals.\n\nScientific Significance and Future Implications\n\nThis trial will be one of the first interventional studies from Pakistan evaluating the impact of non-surgical periodontal therapy on renal function in uncontrolled diabetics. The results could:\n\nProvide evidence to include periodontal screening as part of diabetes management protocols.\n\nSupport collaborative programs between diabetology and dental departments for early detection and management of oral infections.\n\nEncourage larger multicentric clinical trials exploring the long-term effects of periodontal therapy on renal and systemic outcomes in diabetic populations.\n\nThe study's integration of oral health and systemic disease management aligns with global efforts to promote interdisciplinary healthcare and may contribute to policy-level recommendations for diabetic patient care.",[27,33],{"label":28,"type":29,"description":30,"interventionNames":31},"Non-Surgical Periodontal Therapy (Scaling and Root Planing + Oral Hygiene Instructions)","EXPERIMENTAL","Participants in this arm will receive full-mouth non-surgical periodontal therapy, including ultrasonic scaling and manual root planing in a single session performed by trained dental hygienists. This treatment aims to remove supra- and subgingival plaque and calculus to reduce periodontal inflammation. Standardized oral hygiene instructions will also be provided, including demonstration of the Modified Stillman's brushing technique using a soft toothbrush and fluoridated toothpaste twice daily. Participants will be monitored for 90 days to assess changes in renal biomarkers (serum creatinine, blood urea nitrogen, and eGFR)",[32],"Procedure: scaling and root planning",{"label":34,"type":35,"description":36,"interventionNames":37},"Control - Oral Hygiene Instructions with Delayed Periodontal Therapy","ACTIVE_COMPARATOR","Participants in the control arm will receive only standardized oral hygiene instructions at baseline and will not undergo scaling and root planing during the 90-day study period. After completion of follow-up assessments, they will receive the same periodontal therapy as the intervention group (delayed therapy) to ensure ethical equivalence",[32],[39],{"type":40,"name":41,"description":42,"armGroupLabels":43,"otherNames":13},"PROCEDURE","scaling and root planning","Intervention 1: Scaling and Root Planing (SRP) + Oral Hygiene Instructions (OHI)\n\nIntervention Description:\n\nParticipants assigned to the intervention arm will receive full-mouth non-surgical periodontal therapy consisting of scaling and root planning (SRP). Ultrasonic scalers will be used to remove supragingival plaque and calculus, followed by hand instruments (curettes and scalers) for subgingival debridement and root planing. The procedure is performed in a single session by trained and calibrated dental hygienists. Participants will also receive standardized oral hygiene instructions (OHI), including demonstration of the Modified Stillman's toothbrushing technique using a soft-bristle toothbrush and fluoridated toothpaste twice daily. Each participant will be provided with an oral hygiene kit to ensure consistency. Postoperative care includes warm saline rinses for three days. No further periodontal treatment will be given during the 90-day follow-up period.",[34,28],[45],{"name":46,"role":47,"phone":48,"phoneExt":49,"email":50},"Muhammad Ather Khan, BDS","CONTACT","+92-333-2685579","+92-2199232660","ather.khan@duhs.edu.pk",[52],{"facility":53,"status":54,"city":55,"state":56,"zip":57,"country":58,"countryCode":59,"cosmosGeoPoint":60,"geoPoint":65,"contacts":13},"Dow University of Health Scinces","RECRUITING","Karachi","Sindh","75330","Pakistan","PK",{"type":61,"coordinates":62},"Point",[63,64],67.0104,24.8608,{"lat":64,"lon":63},{"type":67,"investigatorFullName":68,"investigatorTitle":69,"investigatorAffiliation":5,"oldNameTitle":13,"oldOrganization":13},"PRINCIPAL_INVESTIGATOR","Dr. Muhammad Ather Khan","Doctor","100612671",false,"NCT07256613","Non-surgical Periodontal Therapy and Kidney Outcomes in Type 2 Diabetes Mellitus","Outcomes of Non-surgical Periodontal Therapy on Urea and Creatinine Levels in Type-2 Diabetes Mellitus Patients","KIDPER","Inclusion Criteria:\n\nAdults between 30 and 65 years of age.\n\nMen and women previously diagnosed with type 2 diabetes mellitus for at least one year.\n\nParticipants with uncontrolled diabetes, defined as HbA1c ≥ 7%.\n\nPresence of moderate to severe gum disease (Stage II or Stage III periodontitis) as determined by a dental examination.\n\nEstimated glomerular filtration rate (eGFR) of 60 mL\u002Fmin\u002F1.73 m² or higher.\n\nWilling and able to provide written informed consent.\n\nExclusion Criteria:\n\nCritically ill individuals or those unable to communicate effectively.\n\nPregnant or breastfeeding women.\n\nWomen currently using hormone replacement therapy or oral contraceptives within the past six months.\n\nIndividuals taking steroidal, nonsteroidal anti-inflammatory drugs (NSAIDs), or other anti-inflammatory medications within the past three months (except low-dose aspirin up to 75 mg daily).\n\nParticipants with a recent history of major blood loss, trauma, or gastrointestinal bleeding.\n\nUse of antibiotics within the last month.\n\nHistory of fever or vomiting lasting more than one week within the last month.\n\nRegular tobacco or alcohol users.\n\nIndividuals with any other chronic disease or condition that could interfere with study outcomes.\n\nIndividuals unwilling or unable to comply with study procedures or follow-up visits.","ALL","30 Years","65 Years",{"count":81,"type":82},46,"ESTIMATED","INTERVENTIONAL",[85],"NA","Brief Summary (Lay Description)\n\nThis research study is being conducted to understand whether treating gum disease (periodontitis) can help improve kidney health in patients who have type-2 diabetes mellitus (T2DM). Both diabetes and gum disease are common long-term conditions that often occur together. People with uncontrolled diabetes are at risk of developing kidney problems due to damage in the small blood vessels of the kidneys - a condition known as diabetic nephropathy.\n\nScientific evidence has already shown that treating gum disease can help improve blood sugar control in diabetic patients. However, it is still unclear whether gum treatment can also help reduce the risk or severity of kidney-related complications. This study aims to find out if non-surgical periodontal therapy (NSPT), which includes scaling and root planing (deep dental cleaning), has any effect on blood markers of kidney function - specifically urea, creatinine, and estimated glomerular filtration rate (eGFR) - in patients with uncontrolled type-2 diabetes.\n\nThe study will be conducted as a randomized controlled trial involving 46 patients with uncontrolled T2DM (HbA1c ≥ 7%) who also have moderate to severe gum disease. Participants will be divided randomly into two groups:\n\nTest Group: Will receive full-mouth non-surgical periodontal therapy (scaling and root planing) and oral hygiene instructions.\n\nControl Group: Will receive oral hygiene instructions only and will get the same gum treatment later (after 90 days, as delayed therapy).\n\nAll participants will have their gum health examined, and blood tests will be done at the start and again after 90 days to measure urea, creatinine, and eGFR levels. These tests help determine how well the kidneys are working. The changes in these values before and after gum treatment will show whether improving oral health has any beneficial impact on kidney function in diabetics.\n\nThe study is expected to take one year and will be conducted at Dow University of Health Sciences, Karachi. All participants will receive standard dental and laboratory assessments at no cost. The results may help improve future strategies for managing diabetic patients by integrating oral health care with medical care.\n\nPurpose:\n\nTo determine whether treating gum disease (through non-surgical periodontal therapy) can improve kidney function markers - urea, creatinine, and eGFR - in patients with uncontrolled type-2 diabetes mellitus.\n\nQuestion being answered:\n\nDoes non-surgical periodontal therapy have a positive effect on kidney function in uncontrolled type-2 diabetic patients by reducing urea and creatinine levels and improving eGFR?",[88,89,90],"Type 2 Diabetes Mellitus MeSH:D003924","Periodontitis MeSH:D010518","Diabetic Nephropathies MeSH:D003928",[92,93,94,95,96,97,98,99,100,101,102,103,104,105,106,107],"Type 2 Diabetes Mellitus","Uncontrolled Type 2 Diabetes","Diabetes-related nephropathy","Chronic kidney disease (CKD)","Diabetic nephropathy","periodontitis","non surgical periodontal therapy","scaling","root palnning","serum creatinine","blood urea nitrogen","BUN","eGFR","MDRD GFR euation","oral hygiene instruction(OHI)","Randomised control trial","2025-11-20",{"date":110,"type":111},"2025-12-01","ACTUAL",{"date":113,"type":111},"2025-08-15",{"date":115,"type":82},"2026-04-15",{"name":5,"class":6},1]