Benign Gynecological Disease

2

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

Condition / disease
Location
Status: Not yet recruiting

Prospective Perioperative Clinical Registry for Women Undergoing Benign Gynecological Surgery

This prospective observational registry aims to systematically collect preoperative, intraoperative, and postoperative clinical data from patients undergoing surgery for benign gynecological conditions. The main goal is to evaluate clinical outcomes, surgical approaches, and complications in real-world clinical practice.

Participants needed: 6,000
Trial details
Age: 18+Biological sex: FemaleType: ObservationalSponsor: IRCCS San RaffaeleUpdated: Aug 19, 2026Locations: 1Duration: 3 Years
Eligibility criteria

Age >= 18 years [+3]

Age < 18 years [+5]

Status: Recruiting

Deep Neuromuscular Blockade and a Low-Residue Diet for the Surgical Field in vNOTES Hysterectomy

vNOTES (vaginal natural orifice transluminal endoscopic surgery) hysterectomy is performed entirely through the vagina, with no abdominal incision. A clear surgical view is essential, and the main obstacle to the view is bowel falling into the pelvis. This randomized trial tests whether two simple measures improve the surgical field, individually or in combination: a preoperative low-residue diet for three days, and deeper intra-operative muscle relaxation (deep neuromuscular blockade). No group receives mechanical bowel preparation. Using a 2×2 factorial design, participants are allocated equally (1:1:1:1) to one of four groups: (1) no diet with standard relaxation; (2) diet with standard relaxation; (3) no diet with deep relaxation; (4) diet with deep relaxation (the "bundle"). The surgical field is measured objectively: during a standardized window the carbon-dioxide insufflation pressure is lowered step by step, and 2-3 blinded assessors score the field from de-identified video. The primary outcome is the lowest pressure at which the field remains adequate; a lower pressure indicates an intrinsically better field. The trial hypothesis is an interaction - that the combination achieves an adequate field at a meaningfully lower pressure than either measure alone. The final sample size is determined from an internal pilot. Secondary outcomes include the continuous field score, the need for an additional instrument to clear the field, postoperative nausea and vomiting, and routine operative outcomes.

Participants needed: 160
Trial details
Age: 18+Biological sex: FemaleType: InterventionalSponsor: Fatih Sultan Mehmet Training and Research HospitalUpdated: Jul 30, 2026Locations: 3
Eligibility criteria

Adult women (aged 18 years or older) scheduled for hysterectomy for a benign (no... [+2]

Suspected or known gynaecological malignancy. [+4]