Clinical Trial

Comparing Intra-Abdominal Pressure During Gynecologic Laparoscopy

Terminated
View on ClinicalTrials.gov →
Why the trial stopped
The hospital closed down the Obstetrics and Gynecology department. Patients relevant to the study are no longer available to recruit.
Summary
The goal of this clinical trial is to learn if the level of intra-abdominal pressure during benign gynecologic laparoscopic surgery impacts postoperative pain. The main question it aims to answer is: • Does use of low (8 mmHg) versus standard (15 mmHg) intra-abdominal pressure impact postoperative pain? Researchers will compare the use of low (8 mmHg) versus standard (15 mmHg) intra-abdominal pressure. Participants will: * Undergo their regular scheduled gynecologic laparoscopic surgery * Complete pain measures one hour, 3 hours, and 24 hours after surgery
Protocol Amendment History 2 amendments
This ClinicalTrials.gov record has been amended 2 times since 2025-10-24; most recent amendment 2026-07-21.
Status change: Not Yet Recruiting → Terminated 2026-07-21
Trial Details
NCT Number NCT07221487
Lead Sponsor Nassau University Medical Center
Conditions Gynecologic Surgical Procedures
Enrollment 37 participants
Start Date 2025-11-23
Primary Completion 2026-07-21 (estimated)
Study Completion 2026-07-21 (estimated)
Updated on ClinicalTrials.gov 2026-07-22