[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"hysteroscopy--methods\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:hysteroscopy--methods":29},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,49],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":30,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":37,"lastUpdatePostDateStruct":38,"startDateStruct":41,"completionDateStruct":43,"leadSponsor":45,"locationsCount":48},"100614945","phase-4-effect-of-misoprostol-on-fluid-deficit-volume-in-hysteroscopic-myomectomy-100614945",false,"NCT07286188","Effect of Misoprostol on Fluid Deficit Volume in Hysteroscopic Myomectomy","Effect of Misoprostol on Fluid Deficit Volume in Hysteroscopic Myomectomy: A Double-Blinded Randomized Controlled Trial","Inclusion Criteria:\n\n* Patients presenting for hysteroscopic myomectomy for uterine fibroids on pelvic imaging (pelvic ultrasound or MRI) within in last 12 months\n* Age ≥ 18 years and ≤ 50 years.\n* Fibroids between 1-3cm in size\n* Myomectomy using myosure or resectoscope devices\n* Willing to have rectal misoprostol or placebo at time of procedure\n* Ability to understand and the willingness to sign a written informed consent.\n* Admissible medical\u002Fsurgical history.\n* Can be previously treated with Depo-Lupron, Depo-Provera, or Oral Contraceptive pills\n* Can have had prior Cesarean delivery\n\nExclusion Criteria:\n\n* Pregnancy. All patients will be required to have a negative urine pregnancy test prior to surgery.\n* Post-menopausal women.\n* Patients with a history of gynecologic malignancy.\n* History of allergic reactions attributed to compounds of similar chemical or biologic composition to misoprostol.\n* Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness\u002Fsocial situations that would limit compliance with study requirements.\n* Known active inflammatory bowel disease involving the rectum or other significant anorectal conditions that may interfere with safe rectal administration of study medication.","FEMALE","18 Years","50 Years",{"count":20,"type":21},40,"ESTIMATED","INTERVENTIONAL",[24],"PHASE4","The goal of this double blinded randomized control trial is to evaluate the impact of misoprostol on fluid deficit during hysteroscopic myomectomies. The main questions it aims to answer are:\n\nIs there is difference in fluid deficit in patients who receive misoprostol vs placebo pre operatively for hysteroscopic myomectomies?\n\nParticipants will be randomized to received 800 mcg of either rectal misoprostol prior to their hysteroscopic myomectomy or 4 tablets of placebo (ZEEBO) prior to their hysteroscopic myomectomy.",[27,28,29],"Fibroids, Uterine","Fluid Deficit","Hysteroscopy \u002F Methods",[31,32,33,34,35],"fibroids","hysteroscopy","myomectomy","fluid deficit","misoprostol","RECRUITING","2026-05-28",{"date":39,"type":40},"2026-06-01","ACTUAL",{"date":42,"type":40},"2025-12-16",{"date":44,"type":21},"2026-12",{"name":46,"class":47},"Northwestern University","OTHER",1,{"id":50,"slug":51,"hasResults":11,"nctId":52,"briefTitle":53,"officialTitle":54,"acronym":55,"eligibilityCriteria":56,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":57,"targetDuration":4,"studyType":22,"phases":59,"briefSummary":61,"conditions":62,"keywords":4,"overallStatus":65,"whyStopped":4,"lastUpdateSubmitDate":66,"lastUpdatePostDateStruct":67,"startDateStruct":69,"completionDateStruct":71,"leadSponsor":73,"locationsCount":4},"100617412","targeted-lidocaine-infusion-for-pain-reduction-in-office-hysteroscopy-100617412","NCT07318285","Targeted Lidocaine Infusion for Pain Reduction in Office Hysteroscopy","A Modified Technique of Target Lidocaine Infusion for Pain Control in Office Hysteroscopy: A Double-Blind Randomized Controlled","OPTILID","Inclusion Criteria:\n\n* Age \\> 18\n* Referred for outpatient diagnostic or operative (see-and-treat) hysteroscopy\n* Able and willing to provide written informed consent\n\nExclusion Criteria:\n\n* Pregnancy\n* Active pelvic inflammatory disease or cervicitis\n* Inability to consent\n* Anti-psychotic drugs usage\n* Previews cervical surgery (i.e., conization).\n* Any contraindication for office hysteroscopy- cervical malignancy, profuse uterine bleeding, invisible external os, recent uterine perforation.\n* Known allergy or hypersensitivity to Lidocaine",{"count":58,"type":21},208,[60],"NA","The goal of this study is to find out whether a small amount of lidocaine (a common local anesthetic) can reduce pain during office hysteroscopy - a procedure used to look inside the uterus. The study will compare lidocaine to saline (salt water) to see which one helps more with pain relief.\n\nParticipants will:\n\n1. Receive either lidocaine or saline gently applied inside the cervix right before the procedure\n2. Undergo the hysteroscopy as planned\n3. Be asked to rate their pain and satisfaction after the procedure\n\nLidocaine is commonly and safely used in dental and gynecological procedures. Participation is voluntary, and the procedure itself will not change.",[29,63,64],"Lidocaine Infusion","Placebo - Control","NOT_YET_RECRUITING","2025-12-28",{"date":68,"type":40},"2026-01-05",{"date":70,"type":21},"2026-02-01",{"date":72,"type":21},"2029-12-30",{"name":74,"class":47},"YAARA TABIB"]