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Comparing Intra-Abdominal Pressure During Gynecologic Laparoscopy

NCT07221487 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 190

Last updated 2025-10-29

No results posted yet for this study

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

Conditions

  • Gynecologic Surgical Procedures

Interventions

PROCEDURE

abdominal pressure

type of intra-abdominal pressure of either standard or low pressure

Sponsors & Collaborators

  • Nassau University Medical Center

    lead OTHER

Principal Investigators

  • Petr Itzhak, DO · Nassau University Medical Center

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-11-30
Primary Completion
2026-05-31
Completion
2026-05-31

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07221487 on ClinicalTrials.gov