[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"gynecologic-disease\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:gynecologic-disease":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,11,0,[8,46,70,93,123,145,169,197,229,256,283],{"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":4,"briefSummary":23,"conditions":24,"keywords":28,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":34,"lastUpdatePostDateStruct":35,"startDateStruct":38,"completionDateStruct":40,"leadSponsor":42,"locationsCount":45},"100579597","immune-cell-populations-in-the-endometrium-100579597",false,"NCT06826365","Immune Cell Populations in the Endometrium","Analysis of Immune Cell Populations in the Endometrium and Peripheral Blood in Women With Reduced and Normal Fertility","Inclusion Criteria:\n\n* age 18-45 years\n* idiopathic infertility\n* at least 2 miscarriages\n* other benign gynecological conditions subjected to endometrial sampling\n\nExclusion Criteria:\n\n* miscarriage within last 3 months\n* abdominal\u002Futerine surgery within last 3 months\n* viral\u002Fbacterial infection within last 3 months\n* antibiotic therapy within last 3 months","FEMALE","18 Years","45 Years",{"count":20,"type":21},50,"ESTIMATED","OBSERVATIONAL","Specialized immunological studies in the diagnostics of idiopathic infertility and recurrent miscarriages have limited applicability, as the role of the immune system in these conditions is not thoroughly understood. In ovulatory cycles, changes occur in the populations of uterine lymphocytes, which may influence the receptivity of the endometrium and the implantation of the embryo. Particularly notable are the changes in natural killer (NK) cells, which reach their peak during the luteal phase and regulate the invasion of the trophoblast. The dominant NK cells exhibit a CD56bright phenotype and differ in cytokine profiles from peripheral blood cells. Cyclical changes also affect macrophages and T lymphocytes; however, it is unclear whether their proportions differ in women with reduced fertility. There is a need to investigate how the composition of lymphocytes in blood influences the populations in the endometrium. The aim of this study is to analyze the correlation between peripheral and endometrial lymphocytes in women with idiopathic infertility and recurrent miscarriages, compared to fertile women.",[25,26,27],"Infertility, Female","Recurrent Miscarriage","Gynecologic Disease",[29,30,31,32],"Idiopathic infertility","Endometrial immunology","Endometrial aspiration biopsy","Recurrent miscarriage","RECRUITING","2026-03-17",{"date":36,"type":37},"2026-03-19","ACTUAL",{"date":39,"type":37},"2025-07-01",{"date":41,"type":21},"2026-06-30",{"name":43,"class":44},"Jagiellonian University","OTHER",1,{"id":47,"slug":48,"hasResults":11,"nctId":49,"briefTitle":50,"officialTitle":50,"acronym":4,"eligibilityCriteria":51,"healthyVolunteers":11,"sex":16,"minAge":52,"maxAge":53,"enrollmentInfo":54,"targetDuration":4,"studyType":56,"phases":57,"briefSummary":59,"conditions":60,"keywords":4,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":61,"lastUpdatePostDateStruct":62,"startDateStruct":64,"completionDateStruct":66,"leadSponsor":68,"locationsCount":45},"100596274","phase-2-clinical-study-to-evaluate-efficacy-of-cabergoline-to-coasting-in-reducing-the-incidence-of-ovarian-hyperstimulation-syndrome-100596274","NCT07043322","Clinical Study to Evaluate Efficacy of Cabergoline to Coasting in Reducing the Incidence of Ovarian Hyperstimulation Syndrome","Inclusion Criteria:\n\n* Age between 18-38 years\n* Body mass index (calculated as weight in kilograms divided by the square of height in meters) \\\u003C 30 kg\u002Fm2.\n* A long luteal protocol is used for ovarian stimulation.\n* Day 2 FSH \\\u003C10 mIU\u002FL and E2\\\u003C 50 pg\u002Fml\n* High risk of OHSS, defined as having more than 20 follicles \\>12 mm in diameter and\u002For E2 levels \\> 3000 pg\u002Fml when the size of the leading follicle is \\> 15 mm\n\nExclusion Criteria:\n\nThe presence of chronic medical diseases, including liver cell failure, renal failure, uncontrolled hypertension, uncontrolled diabetes mellitus, or class 3 or 4 function heart disease in the New York heart association classification.\n\nAllergy to Cabergoline.","20 Years","35 Years",{"count":55,"type":21},150,"INTERVENTIONAL",[58],"PHASE2","Ovarian hyperstimulation syndrome (OHSS) is a serious iatrogenic complication of controlled ovarian stimulation of gonadotrophin-Stimulated ovarian cycles. It is theorized to manifest systemically as a result of vasoactive mediators like vascular endothelium growth factor (VEGF) being released from hyperstimulated ovaries. As a result, capillary permeability is increased which causes the extravasation of fluid from the intravascular compartment into the third space. The haemoconcentration which ensues results in complications such as hypercoagulability and reduced end organ perfusion.",[27],"2026-03-12",{"date":63,"type":37},"2026-03-13",{"date":65,"type":37},"2025-06-30",{"date":67,"type":21},"2026-11-20",{"name":69,"class":44},"Tanta University",{"id":71,"slug":72,"hasResults":11,"nctId":73,"briefTitle":74,"officialTitle":74,"acronym":75,"eligibilityCriteria":76,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":77,"targetDuration":4,"studyType":22,"phases":4,"briefSummary":79,"conditions":80,"keywords":83,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":85,"lastUpdatePostDateStruct":86,"startDateStruct":87,"completionDateStruct":89,"leadSponsor":91,"locationsCount":45},"100595397","ultrasound-image-bank-advancing-medical-research-and-diagnostics-100595397","NCT07031921","Ultrasound Image Bank: Advancing Medical Research and Diagnostics","Ultra-Bank","Inclusion Criteria:\n\n* All patients examined at Class Ultrasound OMIC of Fondazione Policlinico Gemelli, IRCCS in Rome.\n* All patients can be enrolled regardless the results of ultrasound examination: no evidence of disease, suspicion of benign or malignant pathologies\n* Aged ≥ 18 years old\n* Patients who were previously enrolled and their outcome has been completed\n* Signature of informed consent\n\nExclusion Criteria:\n\n* No signed informed consent;",{"count":78,"type":21},25000,"The study titled \"Ultrasound Image Bank: Advancing Medical Research and Diagnostics\", sponsored by the Fondazione Policlinico Universitario A. Gemelli IRCCS, aims to create a large-scale database of gynecological ultrasound images. These images will be collected during routine clinical care from both healthy patients and those with benign or malignant gynecological conditions. The goal is to support medical training, clinical research, and the development of artificial intelligence (AI) models for diagnostic purposes.\n\nThis is a prospective, observational, single-center study, with an expected enrollment of approximately 25,000 patients over five years. The ultrasound images will be linked to histological outcomes (for those undergoing surgery within 3 months) or to follow-up scans at 1 year, to enhance early diagnosis and personalized treatment approaches.",[81,82,27],"Gynecological Imaging","Ultrasound Diagnostics",[84],"Ultrasound Imaging","2026-03-10",{"date":61,"type":37},{"date":88,"type":37},"2025-06-25",{"date":90,"type":21},"2030-05-30",{"name":92,"class":44},"Fondazione Policlinico Universitario Agostino Gemelli IRCCS",{"id":94,"slug":95,"hasResults":11,"nctId":96,"briefTitle":97,"officialTitle":98,"acronym":4,"eligibilityCriteria":99,"healthyVolunteers":11,"sex":16,"minAge":100,"maxAge":4,"enrollmentInfo":101,"targetDuration":4,"studyType":22,"phases":4,"briefSummary":103,"conditions":104,"keywords":109,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":114,"lastUpdatePostDateStruct":115,"startDateStruct":117,"completionDateStruct":119,"leadSponsor":121,"locationsCount":45},"100572088","ultrasound-detection-of-body-composition-in-critical-care-100572088","NCT06728722","Ultrasound Detection of Body Composition in Critical Care","Detection of the Changes in Body Composition of Critically Ill Obstetrics by Ultrasound and the Co-relations With Clinical Outcomes; a Prospective Observational Study.","Inclusion Criteria:\n\n* females with age 16 with no upper limit\n* American Society of Anesthesiologists (ASA) class I, II or III,\n* admitted to the obstetrics and Gynecology critical care unit\n\nExclusion Criteria:\n\n* Patient refusal","16 Years",{"count":102,"type":21},121,"Objective assessment of the Changes in body composition of critically ill patients is very valuable. Ultrasound stands as a solution due to its portability, bedside availability, and radiation-free technology. Those criteria are crucial for critically ill obstetrics and gynecological cases.",[105,106,107,108,27],"Muscle Loss","Extracellular Fluid Alteration","Critical Illness","Pregnancy Complications",[110,111,112,113],"ultrasound","body composition","critical illness","peripartum and gynecological cases","2026-02-08",{"date":116,"type":37},"2026-02-11",{"date":118,"type":37},"2024-12-15",{"date":120,"type":21},"2026-05-28",{"name":122,"class":44},"Ain Shams University",{"id":124,"slug":125,"hasResults":11,"nctId":126,"briefTitle":127,"officialTitle":127,"acronym":4,"eligibilityCriteria":128,"healthyVolunteers":11,"sex":129,"minAge":130,"maxAge":131,"enrollmentInfo":132,"targetDuration":4,"studyType":22,"phases":4,"briefSummary":134,"conditions":135,"keywords":4,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":136,"lastUpdatePostDateStruct":137,"startDateStruct":139,"completionDateStruct":141,"leadSponsor":143,"locationsCount":45},"100608963","awareness-knowledge-and-behavioral-seeking-of-gynaecological-problems-100608963","NCT07208383","Awareness, Knowledge and Behavioral Seeking of Gynaecological Problems","Inclusion Criteria:\n\nAged between 13 and 60 years old\n\nExclusion Criteria:\n\n-Patients unable to provide consent\u002Fassent (i.e. significant psychiatric problems\u002Fcognitive delay)","ALL","13 Years","60 Years",{"count":133,"type":21},800,"This study seeks to fill this gap by examining awareness, knowledge, and help-seeking behaviors among gynecological patients and the general public. By comparing these groups, the study will identify disparities in knowledge and barriers to care, providing insights for targeted interventions to improve women's health outcomes in Hong Kong.",[27],"2026-01-06",{"date":138,"type":37},"2026-01-08",{"date":140,"type":37},"2025-10-21",{"date":142,"type":21},"2037-08-31",{"name":144,"class":44},"Chinese University of Hong Kong",{"id":146,"slug":147,"hasResults":11,"nctId":148,"briefTitle":149,"officialTitle":150,"acronym":4,"eligibilityCriteria":151,"healthyVolunteers":11,"sex":129,"minAge":17,"maxAge":4,"enrollmentInfo":152,"targetDuration":4,"studyType":56,"phases":153,"briefSummary":155,"conditions":156,"keywords":4,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":160,"lastUpdatePostDateStruct":161,"startDateStruct":163,"completionDateStruct":165,"leadSponsor":167,"locationsCount":45},"100596365","molecular-and-cellular-profiling-of-uterine-lavage-collected-during-gynecologic-surgery-100596365","NCT07044505","Molecular and Cellular Profiling of Uterine Lavage Collected During Gynecologic Surgery","Exploring the Molecular and Cellular Composition of Uterine Lavage Specimens Collected at the Time of Gynecologic Surgery.","Inclusion Criteria:\n\n* Undergoing gynecologic surgery with Stanford Healthcare\n* Intact uterus and cervix\n* At least one intact fallopian tube and ovary (on the same side)\n* Aged 18 years or older\n* Ability to understand and the willingness to provide written informed consent.\n\nExclusion Criteria:\n\n* Known endometrial or cervical cancer or endometrial or cervical intraepithelial neoplasia\n* Status post bilateral salpingectomy or tubal ligation\n* Lack of consenting capacity\n* Positive preoperative pregnancy test\n* Active uterine bleeding (i.e. menses, etc.)\n* Intrauterine device in place\n* Non-English speaking (requires interpretor)",{"count":20,"type":21},[154],"NA","This study is a designed as a to test the clinical and technical feasibility of using this novel uterine lavage collection catheter to collected UL samples from up to 50 individuals undergoing gynecologic surgery and to describe the cellular composition of these samples. In order to do this, it is a prospective consecutively-enrolled cohort of 50 participants, all of who will receive the intervention of uterine lavage collection.",[157,27,158,159],"Gynecologic Cancer","Gynecological Surgery","Uterine Cancer","2025-11-03",{"date":162,"type":37},"2025-11-05",{"date":164,"type":37},"2025-09-19",{"date":166,"type":21},"2026-12",{"name":168,"class":44},"Stanford University",{"id":170,"slug":171,"hasResults":11,"nctId":172,"briefTitle":173,"officialTitle":174,"acronym":4,"eligibilityCriteria":175,"healthyVolunteers":11,"sex":16,"minAge":176,"maxAge":177,"enrollmentInfo":178,"targetDuration":4,"studyType":56,"phases":180,"briefSummary":181,"conditions":182,"keywords":184,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":188,"lastUpdatePostDateStruct":189,"startDateStruct":191,"completionDateStruct":193,"leadSponsor":195,"locationsCount":45},"100436477","eras-in-pediatric--adolescent-gynecology-preoperative-counseling-100436477","NCT04963751","ERAS in Pediatric & Adolescent Gynecology Preoperative Counseling","ERAS in Pediatric and Adolescent Gynecology: How Important is Preoperative Counseling in Patient Outcomes and Does Parent Versus Patient Counseling Impact Success?","Inclusion Criteria:\n\n* 9- 17 years of age\n* Patient is undergoing abdominal surgery and being managed under the ERAS protocol\n\nExclusion Criteria:\n\n* Developmental delay (IQ \\\u003C 70) determined by documentation in medical record\n* Emergency or non-elective surgical cases\n* Patients who attend clinic appointments independently from their caregiver","9 Years","17 Years",{"count":179,"type":21},60,[154],"The Investigator propose a randomized trial that will assess whether participant involvement in pre-operative counseling for ERAS improves post-surgical pain scores. The Investigator will also assess participant compliance to ERAS-prescribed medications, and functionality (return to school). Each participant who is enrolled in the study will be assigned to 1) pre-operative counseling with participant's caregiver or 2) caregiver-only counseling.",[183,27],"Enhanced Recovery After Surgery",[185,186,187],"Gynecology","ERAS","Pediatrics","2025-05-05",{"date":190,"type":37},"2025-05-06",{"date":192,"type":37},"2022-09-08",{"date":194,"type":21},"2027-06-30",{"name":196,"class":44},"University of Colorado, Denver",{"id":198,"slug":199,"hasResults":11,"nctId":200,"briefTitle":201,"officialTitle":202,"acronym":4,"eligibilityCriteria":203,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":204,"enrollmentInfo":205,"targetDuration":4,"studyType":56,"phases":207,"briefSummary":208,"conditions":209,"keywords":4,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":220,"lastUpdatePostDateStruct":221,"startDateStruct":223,"completionDateStruct":225,"leadSponsor":227,"locationsCount":45},"100497748","assessment-of-womens-sexual-quality-of-life-after-benign-adnexal-surgery-using-vnotes-approach-100497748","NCT05761275","Assessment of Women's Sexual Quality of Life After Benign Adnexal Surgery Using vNOTES Approach","Assessment of Women's Sexual Quality of Life After Benign Adnexal Surgery Using vNOTES Approach in Comparison to Conventional Laparoscopy: a Randomized Controlled Trial","Inclusion Criteria:\n\n* Women aged from 18 to 70 years\n* Discernment capacity with oral and written consent signed\n* Heterosexual intercourse (with vaginal penetration) within four weeks prior to inclusion in the study\n\nExclusion Criteria:\n\n* History of rectal surgery.\n* Suspected rectovaginal\u002Fretrocervical endometriosis.\n* History of brachytherapy or pelvic radiation.\n* Suspected malignancy.\n* History of severe pelvic inflammatory disease.\n* Active lower genital tract infection.\n* Pregnancy.\n* Women who do not speak fluent French or English.\n* Patients under tutelage (with or without capacity of judgement).","70 Years",{"count":206,"type":21},62,[154],"Transvaginal Natural Orifice Transluminal Endoscopic Surgery (vNOTES) is a recent innovation in minimally invasive surgery which has already proven its non-inferiority to conventional abdominal laparoscopy (CAL) for hysterectomy in terms of efficiency and safety. However, the investigators note a lack of medical literature and no specific randomized controlled trial (RCT) assessing women's sexual function after vNOTES for benign adnexal surgery.\n\nThe aim of this RCT is to confirm the non-inferiority of the vNOTES approach for benign adnexal pathology compared to CAL on women's sexual function. Secondary outcomes will evaluate vNOTES's efficiency, morbidity and postoperative complications compared to CAL for benign adnexal surgery. The relationship between adnexal mass morcellation\u002Faspiration and the quality of the histological analysis on surgical specimens will also be evaluated as secondary outcome.",[27,210,211,212,213,214,215,216,217,218,219],"Adnexal Mass","Adnexal Cyst","Sexuality","Adnexal Diseases","Sexual Dysfunction","Quality of Life","Pathology","Dyspareunia","Pelvic Pain","Complication","2025-03-24",{"date":222,"type":37},"2025-03-27",{"date":224,"type":37},"2024-01-01",{"date":226,"type":21},"2027-04-03",{"name":228,"class":44},"Jean Dubuisson",{"id":230,"slug":231,"hasResults":11,"nctId":232,"briefTitle":233,"officialTitle":234,"acronym":4,"eligibilityCriteria":235,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":236,"targetDuration":4,"studyType":56,"phases":238,"briefSummary":239,"conditions":240,"keywords":241,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":246,"lastUpdatePostDateStruct":247,"startDateStruct":249,"completionDateStruct":251,"leadSponsor":253,"locationsCount":255},"100579135","bowel-preparation-in-minimally-invasive-gynecologic-surgery-100579135","NCT06820359","Bowel Preparation in Minimally Invasive Gynecologic Surgery","Investigating the Necessity of Bowel Preparation in Minimally Invasive Gynecologic Surgery","Inclusion Criteria:\n\n* Scheduled to undergo minimally invasive robotic gynecologic surgery;\n* Age 18 years and above\n* Willing to perform an enema if randomized to the enema group\n* Able to read and understand English\n* Willing to sign an informed consent form\n\nExclusion Criteria:\n\n* Scheduled for open surgery\n* Younger than 18 years of age\n* Unwilling to perform an enema if randomized to the enema group\n* Unable to read and understand English\n* Unwilling to sign an informed consent form",{"count":237,"type":21},166,[154],"This is a prospective randomized study of patients who are scheduled to undergo minimally invasive robotic gynecologic surgery. Patients will be randomized to require either pre-surgical bowel preparation vs. no bowel preparation. The effect of bowel preparation on intraoperative visualization, bowel handling, intestinal load and ease of surgery will be assessed. Patient comfort and satisfaction will be assessed.",[27],[242,243,244,245],"gynecologic surgery","bowel preparation","patient satisfaction","ease of surgery","2025-02-08",{"date":248,"type":37},"2025-02-11",{"date":250,"type":21},"2025-02-17",{"date":252,"type":21},"2026-01-31",{"name":254,"class":44},"Muhammad Aslam",2,{"id":257,"slug":258,"hasResults":11,"nctId":259,"briefTitle":260,"officialTitle":260,"acronym":261,"eligibilityCriteria":262,"healthyVolunteers":263,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":264,"targetDuration":4,"studyType":22,"phases":4,"briefSummary":266,"conditions":267,"keywords":4,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":273,"lastUpdatePostDateStruct":274,"startDateStruct":276,"completionDateStruct":278,"leadSponsor":279,"locationsCount":282},"100546289","evaluation-of-salivary-rna-in-subjects-scheduled-for-surgery-for-a-gynecologic-pathology-100546289","NCT06392997","Evaluation of Salivary RNA in Subjects Scheduled for Surgery for a Gynecologic Pathology","GynRNA","Inclusion Criteria:\n\n1. Subject of legal age (according to local legislation) and at least 18 years old\n2. Subject (and if applicable her legal representative) having dated and signed the informed consent form\n3. Subject with a medical insurance policy\n4. Subject presenting to the department:\n\n   1. With Symptoms (bleeding and\u002For pain and\u002For clinically observed symptom) of one or more of the following pathologies (suspected undergoing diagnostic surgery\u002Fbiopsy or diagnosed and before any curative treatment of the pathology):\n\n      * Endometriosis\n      * Adenomyosis,\n      * Ovarian cysts,\n      * Fibroids,\n      * Ovarian cancer,\n      * Cervical cancer,\n      * Uterine cancer.\n   2. Asymptomatic with pap smear positive for cervical dysplasia or cervical cancer and before any curative treatment.\n   3. Asymptomatic undergoing a pap smear for cervical cancer screening in a gynecological follow-up context.\n\nExclusion Criteria:\n\n1. Recent (\\\u003C1 month) or ongoing bacterial or viral infection\n2. Known active oral or digestive mycosis\n3. Evolving oral pathology, symptomatic or obvious\n4. Known pregnancy\n5. Known current non-gynecological pelvic pathology\n6. Subject with a diagnosed breast cancer or cancer other than gynecological with the exception of basal cell carcinoma\n7. Subject with a history of treated cancer within the last 5 years with the exception of basal cell carcinoma\n8. Subject who has already received chemotherapy or radiotherapy or undergone complete or partial excision of the gynecological pathology of inclusion criterion\n9. Subject with significant difficulties reading or writing her language\n10. Subject unable to comply with study and\u002For follow-up procedures\n11. Participation in an interventional study with investigational drug or in the exclusion period of an interventional study.",true,{"count":265,"type":21},2500,"GynRAN is an international, multicentre, transversal, diagnostic and non-interventional study carried out in gynecology-obstetrics\u002Fgynecological oncology departments that aims to identify a diagnostic signature for gynecological pathologies by analyzing of coding and non-coding RNA contained in patients saliva.\n\nThe study population consists of patients with clinically symptomatic females with one or more of the gynecological pathologies (endometriosis, adenomyosis, ovarian cysts, fibroids, ovarian\u002Fcervical\u002Futerine cancer) and asymptomatic females.\n\nThe patients concerned by the study will be managed without modification of the care pathway, nor modification of the therapeutic indications, nor modification of the diagnostic or follow-up examinations necessary according to the context, which are carried out according to the local recommendations.",[27,157,268,269,270,271,272,159],"Endometriosis","Ovarian Cancer","Cyst Ovary","Fibroid","Cervical Cancer","2025-01-20",{"date":275,"type":37},"2025-01-23",{"date":277,"type":37},"2024-12-05",{"date":166,"type":21},{"name":280,"class":281},"ZIWIG","INDUSTRY",13,{"id":284,"slug":285,"hasResults":11,"nctId":286,"briefTitle":287,"officialTitle":288,"acronym":289,"eligibilityCriteria":290,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":291,"enrollmentInfo":292,"targetDuration":4,"studyType":56,"phases":294,"briefSummary":295,"conditions":296,"keywords":4,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":300,"lastUpdatePostDateStruct":301,"startDateStruct":303,"completionDateStruct":305,"leadSponsor":307,"locationsCount":45},"100514169","robotic-assisted-versus-conventional-laparoscopic-surgery-in-obese-patients-with-early-endometrial-cancer-100514169","NCT05974995","Robotic-assisted Versus Conventional Laparoscopic Surgery in Obese Patients With Early Endometrial Cancer","Robotic-assisted Versus Conventional Laparoscopic Surgery in the Management of Obese Patients With Early Endometrial Cancer in the Sentinel Lymph Node Era: a Randomized Controlled Study","RObese","Inclusion Criteria:\n\n* BMI \\>=30\n* Age \\> 18\n* Histologically confirmed endometrioid endometrial cancer\n* Clinical early stage (stage I)\n* No contraindication for minimally invasive surgery\n* ASA\\\u003C4\n* Written informed consent.\n\nExclusion Criteria:\n\n* High probability of laparotomy related to uterine volume (US estimated weight \\>250 g)\n* Concomitant pelvic disease, or anatomical characteristics of the patient\n* (Use of uterine manipulator)\n* Age \\>75 years","75 Years",{"count":293,"type":21},566,[154],"Data across literature suggest that robotic surgery may offer benefit specifically in patient with morbid obesity with endometrial cancer, but to date no randomized trials have been conducted to confirm these observations.\n\nThis randomized controlled multicentric trial aims to evaluate the most appropriate minimally invasive surgical approach in morbidly obese (BMI \\>= 30) patients with endometrial carcinoma.",[297,298,299,157,27],"Endometrial Cancer","Endometrial Neoplasms","Obesity, Morbid","2024-10-01",{"date":302,"type":37},"2024-10-03",{"date":304,"type":37},"2023-09-01",{"date":306,"type":21},"2029-09-01",{"name":92,"class":44}]