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ACTIVE NOT RECRUITING
NCT06909058
NA

Postoperative Restrictions for Patients Undergoing Minimally Invasive Gynecologic Procedures

Sponsor: Anna Frappaolo

View on ClinicalTrials.gov

Summary

The goal of this randomized controlled trial is to assess recovery in patients undergoing benign laparoscopic gynecologic surgery. The main question it aims to answer is: do liberalized postoperative restrictions improve patient recovery after laparoscopic gynecologic surgery? Researchers will compare postoperative recovery surveys from the control group (patients given standard postoperative restrictions limiting activity for 2 weeks) to the research group (patients given liberalized postoperative instructions allowing them to engage in their normal activities of daily life at their own discretion without prescribed activity restrictions) to see if liberalized postoperative restrictions improve the recovery experience. Participants will be asked to fill out a brief questionnaire at two time intervals, 1 week after surgery and 2 weeks after surgery.

Key Details

Gender

FEMALE

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

148

Start Date

2025-04-07

Completion Date

2026-07-01

Last Updated

2026-04-07

Healthy Volunteers

Yes

Interventions

BEHAVIORAL

Study Postoperative Care

The study group will be given general postoperative instructions. They will also receive liberal activity restrictions instructing the patient to resume normal activities of daily living at their own discretion without specific restrictions.

Locations (1)

Women and Infants Hospital

Providence, Rhode Island, United States