Gynecologic Disease

11

Review clinical trials related to Gynecologic Disease. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Immune Cell Populations in the Endometrium

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.

Participants needed: 50
Trial details
Age: 18-45Biological sex: FemaleType: ObservationalSponsor: Jagiellonian UniversityUpdated: Mar 19, 2026Locations: 1
Eligibility criteria

age 18-45 years [+3]

miscarriage within last 3 months [+3]

Status: Recruiting

Clinical Study to Evaluate Efficacy of Cabergoline to Coasting in Reducing the Incidence of Ovarian Hyperstimulation Syndrome

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.

Participants needed: 150
Trial details
Phase: Phase 2Age: 20-35Biological sex: FemaleType: InterventionalSponsor: Tanta UniversityUpdated: Mar 13, 2026Locations: 1
Eligibility criteria

Age between 18-38 years [+4]

Status: Recruiting

Ultrasound Image Bank: Advancing Medical Research and Diagnostics

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. This 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.

Participants needed: 25,000
Trial details
Age: 18+Biological sex: FemaleType: ObservationalSponsor: Fondazione Policlinico Universitario Agostino Gemelli IRCCSUpdated: Mar 12, 2026Locations: 1
Eligibility criteria

All patients examined at Class Ultrasound OMIC of Fondazione Policlinico Gemelli... [+4]

No signed informed consent;

Status: Recruiting

Ultrasound Detection of Body Composition in Critical Care

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.

Participants needed: 121
Trial details
Age: 16+Biological sex: FemaleType: ObservationalSponsor: Ain Shams UniversityUpdated: Feb 11, 2026Locations: 1
Eligibility criteria

females with age 16 with no upper limit [+2]

Patient refusal

Status: Recruiting

Awareness, Knowledge and Behavioral Seeking of Gynaecological Problems

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.

Participants needed: 800
Trial details
Age: 13-60Biological sex: AllType: ObservationalSponsor: Chinese University of Hong KongUpdated: Jan 8, 2026Locations: 1
Eligibility criteria

Not listed

Status: Recruiting

Molecular and Cellular Profiling of Uterine Lavage Collected During Gynecologic Surgery

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.

Participants needed: 50
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Stanford UniversityUpdated: Nov 5, 2025Locations: 1
Eligibility criteria

Undergoing gynecologic surgery with Stanford Healthcare [+4]

Known endometrial or cervical cancer or endometrial or cervical intraepithelial... [+6]

Status: Recruiting

ERAS in Pediatric & Adolescent Gynecology Preoperative Counseling

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.

Participants needed: 60
Trial details
Age: 9-17Biological sex: FemaleType: InterventionalSponsor: University of Colorado, DenverUpdated: May 6, 2025Locations: 1
Eligibility criteria

9- 17 years of age [+1]

Developmental delay (IQ < 70) determined by documentation in medical record [+2]

Status: Recruiting

Assessment of Women's Sexual Quality of Life After Benign Adnexal Surgery Using vNOTES Approach

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. The 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/aspiration and the quality of the histological analysis on surgical specimens will also be evaluated as secondary outcome.

Participants needed: 62
Trial details
Age: 18-70Biological sex: FemaleType: InterventionalSponsor: Jean DubuissonUpdated: Mar 27, 2025Locations: 1
Eligibility criteria

Women aged from 18 to 70 years [+2]

History of rectal surgery. [+8]

Status: Recruiting

Bowel Preparation in Minimally Invasive Gynecologic Surgery

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.

Participants needed: 166
Trial details
Age: 18+Biological sex: FemaleType: InterventionalSponsor: Muhammad AslamUpdated: Feb 11, 2025Locations: 2
Eligibility criteria

Scheduled to undergo minimally invasive robotic gynecologic surgery; [+4]

Scheduled for open surgery [+4]

Status: Recruiting

Evaluation of Salivary RNA in Subjects Scheduled for Surgery for a Gynecologic Pathology

GynRAN is an international, multicentre, transversal, diagnostic and non-interventional study carried out in gynecology-obstetrics/gynecological oncology departments that aims to identify a diagnostic signature for gynecological pathologies by analyzing of coding and non-coding RNA contained in patients saliva. The study population consists of patients with clinically symptomatic females with one or more of the gynecological pathologies (endometriosis, adenomyosis, ovarian cysts, fibroids, ovarian/cervical/uterine cancer) and asymptomatic females. The 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.

Participants needed: 2,500
Trial details
Age: 18+Biological sex: FemaleType: ObservationalSponsor: ZIWIGUpdated: Jan 23, 2025Locations: 13
Eligibility criteria

Subject of legal age (according to local legislation) and at least 18 years old [+11]

Recent (<1 month) or ongoing bacterial or viral infection [+10]

Status: Recruiting

Robotic-assisted Versus Conventional Laparoscopic Surgery in Obese Patients With Early Endometrial Cancer

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. This randomized controlled multicentric trial aims to evaluate the most appropriate minimally invasive surgical approach in morbidly obese (BMI \>= 30) patients with endometrial carcinoma.

Participants needed: 566
Trial details
Age: 18-75Biological sex: FemaleType: InterventionalSponsor: Fondazione Policlinico Universitario Agostino Gemelli IRCCSUpdated: Oct 3, 2024Locations: 1
Eligibility criteria

BMI >=30 [+6]

High probability of laparotomy related to uterine volume (US estimated weight >2... [+3]