Comparing Intra-Abdominal Pressure During Gynecologic Laparoscopy

Conditions

• Gynecologic Surgical Procedures

Eligibility Criteria

Sex

FEMALE

Age

18 Years - N/A

Healthy Volunteers

Not accepted

Interventions

• abdominal pressure — PROCEDURE
  type of intra-abdominal pressure of either standard or low pressure

Study Details

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

Key Dates

Start date

Nov 30, 2025

Status verified

Oct 2025

Primary completion

May 31, 2026

Completion

May 31, 2026

Study Design

Enrollment

190 participants (estimated)

Allocation

RANDOMIZED

Intervention model

PARALLEL

Primary purpose

TREATMENT

Arms

• Active Comparator: standard-pressure group
  15 mmHg pressure
• Experimental: low-pressure group
  8 mmHg

Primary Outcome Measure

PAIN OUT questionnaire [ Time Frame: Perioperative/Periprocedural: Three hours after surgery completed ]

Central Contacts

• Petr Itzhak, DO
  516-296-7394
  [email protected]

Locations (1)

Find similar trials in East Meadow, NY

Related Studies

• Intraperitoneal Infusion of Analgesic for Postoperative Pain Management
  PHASE4 · Recruiting · Ying Liu · Washington D.C., District of Columbia