[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"abortion-spontaneous\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:abortion-spontaneous":41},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,1,0,[8],{"id":9,"slug":4,"hasResults":10,"nctId":11,"briefTitle":12,"officialTitle":13,"acronym":4,"eligibilityCriteria":14,"healthyVolunteers":15,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":4,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":30,"lastUpdatePostDateStruct":31,"startDateStruct":34,"completionDateStruct":36,"leadSponsor":38,"locationsCount":5},"100569617",false,"NCT06696573","Effectiveness of Anti-Inflammatory Drugs for Preventing Pain Versus Treating Pain During Medical Abortion From 13 to 22 Weeks at Hung Vuong Hospital","Effectiveness of Proactive Versus On-Demand Pain Relief With Non-Steroidal Anti-Inflammatory Drugs During Medical Abortion at 13 to 22 Weeks at Hung Vuong Hospital","Inclusion Criteria:\n\n* Pregnant women aged 18 years or older.\n* No mental illness.\n* Gestational age between 13 and 22 weeks (based on the last menstrual period with a regular menstrual cycle and accurate recall of the last menstrual period, or based on a first-trimester ultrasound) with an indication of stillbirth, fetal malformation requiring termination, or voluntary abortion with counseling and understanding of the abortion procedure.\n* Willing to participate in the study.\n* Capable of reading and signing the informed consent form.\n* Able to provide personal information independently.\n\nExclusion Criteria:\n\n* Medical conditions contraindicating medical abortion: bleeding disorders, anticoagulant use, moderate to severe anemia.\n* Cardiovascular conditions: heart failure, mitral valve stenosis, embolism, uncontrolled hypertension.\n* Other medical conditions: renal failure, adrenal gland disorders, severe asthma, liver and biliary diseases, glaucoma.\n* Active pelvic inflammatory disease or acute genital infections.\n* Previous uterine surgery.\n* Placenta previa or central placenta previa.\n* Uterine malformations.\n* History of allergy to NSAIDs, Mifepristone, or Misoprostol.\n* Unwillingness to participate in the study.",true,"FEMALE","18 Years",{"count":19,"type":20},180,"ESTIMATED","INTERVENTIONAL",[23],"NA","The goal of this clinical trial is to assess the effectiveness of non-steroidal anti-inflammatory drugs (NSAIDs) for prophylactic pain relief compared to on-demand pain relief during medical abortion for pregnancies between 13 and 22 weeks at Hung Vuong Hospital in Ho Chi Minh City. The main questions it aims to answer are:\n\n1. Does prophylactic use of NSAIDs reduce pain compared to on-demand use during medical abortion?\n2. What are the potential adverse effects of NSAIDs in this context?\n\nResearchers will compare a group receiving prophylactic NSAIDs to a control group receiving on-demand pain relief to determine if the prophylactic approach leads to improved pain management outcomes.\n\nParticipants will:\n\n* Be given NSAIDs either as a preventative measure or upon the onset of pain.\n* Be monitored for pain levels using validated pain scales, any side effects, and outcomes of the abortion procedure.",[26,27,28],"Pain Management","Anti-Inflammatory Agents, Non-Steroidal","Abortion, Spontaneous","RECRUITING","2025-03-10",{"date":32,"type":33},"2025-03-13","ACTUAL",{"date":35,"type":33},"2024-12-13",{"date":37,"type":20},"2025-12",{"name":39,"class":40},"Le Thi Kieu Trang","OTHER",""]