[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"pain-associated-with-intrauterine-device-insertion\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:pain-associated-with-intrauterine-device-insertion":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,1,0,[8],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":29,"overallStatus":39,"whyStopped":4,"lastUpdateSubmitDate":40,"lastUpdatePostDateStruct":41,"startDateStruct":44,"completionDateStruct":46,"leadSponsor":48,"locationsCount":5},"100658685","li4-acupuncture-for-pain-during-intrauterine-device-insertion-100658685",false,"NCT07854015","LI4 Acupuncture for Pain During Intrauterine Device Insertion","Effect of Acupuncture at the LI4 Point on Pain During Intrauterine Device Insertion: A Sham-Controlled Randomized Clinical Trial","Inclusion Criteria:\n\n* Women aged 18-50 years\n* Scheduled to undergo copper intrauterine device (IUD) insertion for contraception\n* Able to communicate in Turkish\n* Able to understand and use the Visual Analog Scale (VAS) for pain assessment\n* Able and willing to provide written informed consent\n\nExclusion Criteria:\n\n* Confirmed or suspected pregnancy\n* Active pelvic infection\n* Unexplained abnormal uterine bleeding\n* Any contraindication to IUD insertion\n* Use of opioid analgesic or sedative medication within the preceding 24 hours\n* Known allergy or hypersensitivity to acupuncture needle materials\n* Needle phobia\n* Infection, wound, or other significant skin lesion at or near the acupuncture site\n* Serious psychiatric disorder or cognitive impairment that may interfere with pain assessment or study participation\n* Neurological disease or sequelae that may interfere with pain perception or pain assessment\n* Requirement for an emergency procedure\n* Previous participation in this study",true,"FEMALE","18 Years","50 Years",{"count":21,"type":22},150,"ESTIMATED","INTERVENTIONAL",[25],"NA","This study will evaluate whether acupuncture can reduce pain during intrauterine device (IUD) insertion. Women undergoing IUD insertion will be randomly assigned to receive either real acupuncture at the LI4 point on both hands or a sham acupuncture procedure that does not penetrate the skin. Both interventions will be applied for 15 minutes before IUD insertion. Participants will not know which treatment they receive. The clinician performing the IUD insertion and the researcher assessing the outcomes will also be unaware of the treatment assignment. Pain will be measured at different stages of the IUD insertion procedure and shortly after the procedure. The main outcome will be the highest pain score reported during IUD insertion. The study will also assess procedure tolerance, patient satisfaction, need for additional pain medication, and adverse events.",[28],"Pain Associated With Intrauterine Device Insertion",[30,31,32,33,34,35,36,37,38],"Acupuncture","LI4","Hegu","Intrauterine Device","IUD Insertion","Procedural Pain","Pain Management","Sham Acupuncture","Park Sham Device","NOT_YET_RECRUITING","2026-09-27",{"date":42,"type":43},"2026-10-02","ACTUAL",{"date":45,"type":22},"2026-10-15",{"date":47,"type":22},"2027-05-01",{"name":49,"class":50},"Nigde Omer Halisdemir University","OTHER"]