[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100506651":3},{"organization":4,"outcomesModule":7,"designInfo":33,"detailedDescription":36,"studyPopulation":37,"armGroups":32,"interventions":32,"overallOfficials":38,"centralContacts":42,"locations":50,"responsibleParty":98,"collaborators":100,"id":103,"slug":32,"hasResults":104,"nctId":105,"briefTitle":106,"officialTitle":107,"acronym":108,"eligibilityCriteria":109,"healthyVolunteers":104,"sex":110,"minAge":111,"maxAge":32,"enrollmentInfo":112,"targetDuration":32,"studyType":115,"phases":32,"briefSummary":116,"conditions":117,"keywords":32,"overallStatus":72,"whyStopped":32,"lastUpdateSubmitDate":122,"lastUpdatePostDateStruct":123,"startDateStruct":126,"completionDateStruct":128,"leadSponsor":130,"locationsCount":131},{"fullName":5,"class":6},"University of Aberdeen","OTHER",{"primaryOutcomes":8,"secondaryOutcomes":13,"otherOutcomes":32},[9],{"measure":10,"description":11,"timeFrame":12},"Patient reported Opioid use post surgery","Patient reported use of opioids post surgery","3 months",[14,18,20,22,26,29],{"measure":15,"description":16,"timeFrame":17},"Opioid use","Patient reported use of opioids pre-op and opioids used during surgery and prescribed post surgery","From recruitment to 1 year post surgery",{"measure":19,"description":19,"timeFrame":17},"Patient reported incidence of pain pre-op and post surgery using BPI-SF",{"measure":21,"description":21,"timeFrame":17},"Patient reported incidence of pain pre-op and post surgery using DN2",{"measure":23,"description":24,"timeFrame":25},"Surgical complications","Recording of surgical complications during surgery","During surgery",{"measure":27,"description":28,"timeFrame":17},"Participant reported quality of life EQ5D-5L","EQ5D-5L",{"measure":30,"description":31,"timeFrame":17},"Participant reported quality of life BPI-SF","BPI-SF",null,{"allocation":32,"interventionModel":32,"interventionModelDescription":32,"primaryPurpose":32,"observationalModel":34,"timePerspective":35,"maskingInfo":32},"ECOLOGIC_OR_COMMUNITY","PROSPECTIVE","PANDOS is an international, prospective, observational cohort study. In a one week period (the designated \"study week\"), data will be collected in all eligible hospitalised adult patients who undergo surgery in as many hospitals as possible in the UK and Europe. Participants will be followed up for 12 months","All eligible patients undergoing surgery at the hospital during the designated study week",[39],{"name":40,"affiliation":5,"role":41},"Patrice Forget","PRINCIPAL_INVESTIGATOR",[43,47],{"name":40,"role":44,"phone":45,"phoneExt":32,"email":46},"CONTACT","01224437285","patrice.forget@abdn.ac.uk",{"name":48,"role":44,"phone":32,"phoneExt":32,"email":49},"Holly R Keir, PhD","PANDOS@abdn.ac.uk",[51,70,81,90],{"facility":52,"status":53,"city":54,"state":55,"zip":56,"country":57,"countryCode":58,"cosmosGeoPoint":59,"geoPoint":64,"contacts":65},"Department of Anaesthesiology Sestre Milosrdnice, University Hospital Center","NOT_YET_RECRUITING","Zagreb","Vinogradska 29","10000","Croatia","HR",{"type":60,"coordinates":61},"Point",[62,63],15.97798,45.81444,{"lat":63,"lon":62},[66],{"name":67,"role":44,"phone":68,"phoneExt":32,"email":69},"Tomislav Radocaj","+38591 1262 586","tomislav.radocaj@kbcsm.hr",{"facility":71,"status":72,"city":73,"state":32,"zip":32,"country":74,"countryCode":75,"cosmosGeoPoint":76,"geoPoint":80,"contacts":32},"NHS Grampian","RECRUITING","Aberdeen","United Kingdom","UK",{"type":60,"coordinates":77},[78,79],-2.09814,57.14369,{"lat":79,"lon":78},{"facility":82,"status":83,"city":84,"state":32,"zip":32,"country":74,"countryCode":75,"cosmosGeoPoint":85,"geoPoint":89,"contacts":32},"University College London Hospitals NHS Foundation Trust","ACTIVE_NOT_RECRUITING","London",{"type":60,"coordinates":86},[87,88],-0.12574,51.50853,{"lat":88,"lon":87},{"facility":91,"status":83,"city":92,"state":32,"zip":32,"country":74,"countryCode":75,"cosmosGeoPoint":93,"geoPoint":97,"contacts":32},"Kings Mill Hospital, Sherwood Forest Hospitals NHS Foundation Trust","Nottingham",{"type":60,"coordinates":94},[95,96],-1.15047,52.9536,{"lat":96,"lon":95},{"type":99,"investigatorFullName":32,"investigatorTitle":32,"investigatorAffiliation":32,"oldNameTitle":32,"oldOrganization":32},"SPONSOR",[101],{"name":102,"class":6},"European Society of Anaesthesiology and Intensive Care","100506651",false,"NCT05877157","Pain AND Opioids After Surgery","Pain and Opioids After Surgery (PANDOS) Study","PANDOS","Inclusion Criteria:\n\n* hospitalised adult patients (18 years and older) undergoing any inpatient surgery (elective or emergency) during the designated study week where an anaesthetist is involved (general anaesthetic, sedation, local anaesthetic).\n\nAble to understand and has capacity to give written informed consent\n\nExclusion Criteria:\n\n* American Society of Anaesthesiologists (ASA) grade V or VI\n* Refusal to participate.\n* Lack of comprehension of validated questionnaires or inability to complete the follow-up for any reason.\n* Lack of capacity to give written informed consent","ALL","18 Years",{"count":113,"type":114},10000,"ESTIMATED","OBSERVATIONAL","The aim of this study is to document the perioperative opioid use and its safety in the UK and countries in Europe and to describe its association with surgical complications, persistent pain and quality of life. In an international, prospective, observational cohort study, data about the perioperative pain management will be collected in all eligible hospitalised adult patients who undergo surgery in a designated \"study week\" in as many hospitals as possible in Europe. Baseline data will be collected, and participants followed up at one week, and at three and twelve months post-operatively. The primary outcome will be opioid use at three months after surgery. Secondary outcomes will include opioid use during the preoperative month (preoperative use), during surgery and up to one week after surgery (or discharge, whichever is earlier), and up to the end of the postoperative year. Additional secondary outcomes are the incidence of preoperative pain, persistent pain with\u002Fwithout the presence of neuropathic components, quality of life and surgical complications. The potential association between opioid use and pain outcomes will be investigated. This study could help to develop strategies to improve quality of care, through pain management, for patients undergoing surgery.",[118,119,120,121],"Opioid Use","Pain, Chronic","Pain, Postoperative","Quality of Life","2024-12-18",{"date":124,"type":125},"2024-12-24","ACTUAL",{"date":127,"type":125},"2023-09-25",{"date":129,"type":114},"2026-09-30",{"name":5,"class":6},4]