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NCT06909058 · ClinicalTrials.gov registry record · NA
Postoperative Restrictions for Patients Undergoing Minimally Invasive Gynecologic Procedures
A NA study of Postoperative Care and MIGS, sponsored by Anna Frappaolo.
- Active
- Registry status
- NA
- Development phase
- 148
- Enrollment target
- 1
- Study location
NCT06909058: Active NA study of Postoperative Care and MIGS, sponsored by Anna Frappaolo.
NCT06909058 is a NA study of Postoperative Care and MIGS that is active but no longer recruiting, run by Anna Frappaolo. The registered enrollment target is 148 participants, above the 110-participant average among 4 other Postoperative Care trials with a reported enrollment target (35% higher). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT06909058, a NA study of Postoperative Care and MIGS, is active but no longer recruiting, sponsored by Anna Frappaolo.
- ACTIVE NOT RECRUITING
- Registry status
- NA
- Development phase
- 148 participants
- Enrollment target
- 1
- Study location
Study 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.
Primary Outcome
Postoperative recovery will be evaluated using the Recovery Index-10 (RI-10), a recovery-specific instrument to assess subjective postoperative recovery that is specifically validated for gynecologic surgery. It is graded on a 5-point numerical Likert scale ranging from "full disagreement" to "full agreement." The questionnaire asks questions regarding pain, stamina/ability to complete daily chores, energy, and sleep. Prior literature on the use and validation of RI-10 suggests a standard deviat
Conditions Studied
Interventions
- BEHAVIORAL Study Postoperative Care
Study Locations (1)
Rhode Island
- Women and Infants Hospital - Providence
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 148 participants |
| Start Date | 2025-04-07 |
| Est. Completion | 2026-02-01 |
| Phase | NA |
What the registry record for NCT06909058 still lists
NCT06909058 is an interventional study that assigns participants to a tested intervention. The registered 148 participants enrollment target is mid-sized for trials with a published cap, above the 110-participant average among 4 other Postoperative Care trials with a reported enrollment target (35% higher).
The record links to 2 conditions, with Postoperative Care appearing as the primary indexed condition, and to 1 intervention - of which Study Postoperative Care is the first listed.
NCT06909058 reports a single indexed study location in Rhode Island.
Frequently Asked Questions
What is clinical trial NCT06909058 about?
NCT06909058 is a clinical study titled "Postoperative Restrictions for Patients Undergoing Minimally Invasive Gynecologic Procedures". 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 comp...
What is the current status of trial NCT06909058?
This trial is currently active not recruiting. It is a NA study. The enrollment target is 148 participants. The study started on 2025-04-07. Estimated completion is 2026-02-01.
What conditions does trial NCT06909058 study?
This clinical trial studies the following conditions: Postoperative Care, MIGS.
What interventions are being tested in trial NCT06909058?
The interventions under investigation include: Study Postoperative Care (BEHAVIORAL).
Who is sponsoring clinical trial NCT06909058?
This trial is sponsored by Anna Frappaolo, which has 1 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06909058 being conducted?
This trial has 1 study location across Rhode Island. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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