[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"endometrial-polyps\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:endometrial-polyps":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,44],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":14,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":4,"briefSummary":23,"conditions":24,"keywords":28,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":32,"lastUpdatePostDateStruct":33,"startDateStruct":36,"completionDateStruct":38,"leadSponsor":40,"locationsCount":43},"100596658","cohort-study-of-intrauterine-diseases-100596658",false,"NCT07048327","Cohort Study of Intrauterine Diseases","TJ Intrauterin","Inclusion Criteria:\n\n* Age: 18-80 years;\n* Patients requiring hysteroscopy or diagnostic curettage for intrauterine pathologies (e.g., endometrial hyperplasia, endometrial polyps, submucosal uterine fibroids, adenomyosis, or endometrial malignancies);\n* Willing and able to comply with follow-up requirements;\n* Signed informed consent obtained.\n\nExclusion Criteria:\n\n* Concurrent participation in other drug clinical trials;\n* Contraindications to or inability to tolerate hysteroscopy\u002Fcurettage procedures;\n* Unwilling or unable to provide informed consent;\n* Unwilling or unable to adhere to study protocols.","FEMALE","18 Years","80 Years",{"count":20,"type":21},2000,"ESTIMATED","OBSERVATIONAL","\"This study employs a prospective cohort design by establishing a uterine cavity diseases research platform. The investigators will collect participants' current medical history, menstrual and obstetric history, past medical history, physical and gynecological examinations, imaging studies, laboratory tests, and pathological examinations. After the hysteroscopic surgery, the investigators will conduct a one-year follow-up on the disease progression of the participants. Through this comprehensive approach, the investigators aim to deeply investigate the pathogenesis, risk factors, and optimized treatment strategies for uterine cavity diseases.\"",[25,26,27],"Endometrial Cancer","Endometrial Hyperplasia","Endometrial Polyps",[29,25,26,27,30],"Intrauterine diseases","Cohort Study","RECRUITING","2025-06-24",{"date":34,"type":35},"2025-07-02","ACTUAL",{"date":37,"type":21},"2025-07",{"date":39,"type":21},"2028-07",{"name":41,"class":42},"Wenwen Wang","OTHER",1,{"id":45,"slug":46,"hasResults":11,"nctId":47,"briefTitle":48,"officialTitle":49,"acronym":4,"eligibilityCriteria":50,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":51,"targetDuration":4,"studyType":53,"phases":54,"briefSummary":56,"conditions":57,"keywords":4,"overallStatus":61,"whyStopped":4,"lastUpdateSubmitDate":62,"lastUpdatePostDateStruct":63,"startDateStruct":65,"completionDateStruct":67,"leadSponsor":69,"locationsCount":4},"100563808","impact-of-different-saline-pressures-during-hysteroscopy-on-visibility-feasibility-and-patients-discomfort-100563808","NCT06620978","Impact of Different Saline Pressures During Hysteroscopy on Visibility, Feasibility and Patients' Discomfort","Operative Hysteroscopy Without Anaesthesia: Impact of Different Distention Medium Pressure (Using Normal Saline) on Visibility, Feasibility and Patients' Discomfort","Inclusion Criteria:\n\n1. Women age \\>18 years\n2. Willing to undergo operative hysteroscopy without anesthesia for\n\nThe following intrauterine findings:\n\nA. Endometrial polyps \\<1.5 cm B. Retained products of conception \\<1.5 cm C. Lysis of intrauterine adhesions D. Removal of retained intrauterine device\n\nExclusion Criteria:\n\n1. Contraindication for hysteroscopy including: suspected pregnancy, heavy concomitant vaginal bleeding, known genital tract malignancy, suspected concurrent genital tract infection.\n2. Unable to sign informed consent\n3. Unable to read\u002Fwrite Hebrew",{"count":52,"type":21},100,"INTERVENTIONAL",[55],"NA","Hysteroscopy is a minimally invasive diagnostic and therapeutic procedure for various intrauterine conditions. It is performed with an optic device while entering liquid media to the uterus to allow visualization. Diagnostic procedures are often performed without anaesthesia (in the office setting) and operative procedures are performed either under general anaesthesia or without anaesthesia (in the office setting). It depends on the patients' characteristics and preferences, and surgical indications. 80%-100% of operative procedure without anesthesia can be successfully completed. The main reasons for inability to successfully complete operative hysteroscopy without anesthesia are patients' discomfort and limited visibility of the uterine cavity.\n\nIn the current study, the investigators will compare the use of two different pressure setting of the liquid media during operative hysteroscopy without anesthesia, with the aim of investigating the successful completion of the procedure and patient's discomfort, with the aim of determining the optimal pressure setting.",[27,58,59,60],"Retained Products of Conception","Lysis of Intrauterine Adhesions","Removal of Retained Intrauterine Device","NOT_YET_RECRUITING","2024-10-01",{"date":64,"type":35},"2024-10-02",{"date":66,"type":21},"2024-11-01",{"date":68,"type":21},"2025-12-31",{"name":70,"class":71},"Assaf-Harofeh Medical Center","OTHER_GOV"]