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NCT03836365 · ClinicalTrials.gov registry record · NA
Patient Preparedness for Pelvic Organ Prolapse Surgery
A NA study, sponsored by University of Pittsburgh.
- Completed
- Registry status
- NA
- Development phase
- 120
- Enrollment target
NCT03836365 is a NA study that has completed, run by University of Pittsburgh. The registered enrollment target is 120 participants.
The verdict
NCT03836365, a NA study, has completed, sponsored by University of Pittsburgh.
- COMPLETED
- Registry status
- NA
- Development phase
- 120 participants
- Enrollment target
Study Summary
Patient preparedness has been associated with increased patient satisfaction, decreased postoperative pain and decreased postoperative narcotic use; however, little is known regarding the optimal way to prepare patients prior to pelvic reconstructive surgery. The primary aim of this study is to determine if a preoperative counseling in person visit has similar rates of patient preparedness as a preoperative counseling phone call for women undergoing same-day pelvic organ prolapse surgery. Secondary aims evaluate patient satisfaction, postoperative pain scores and postoperative narcotic usage. Women who plan to undergo pelvic organ prolapse surgery will be randomized to a preoperative in person counseling visit or a preoperative counseling phone call. Participants will complete questionnaires to assess their preparedness, satisfaction and postoperative pain. The goal of this study is to gather information that will allow clinicians to improve patient surgical preparedness and satisfaction.
Interventions
- OTHER Preoperative counseling office visit
- OTHER Preoperative counseling phone call
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 120 participants |
| Start Date | 2019-04-02 |
| Est. Completion | 2020-05-01 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03836365
The ClinicalTrials.gov registry entry for NCT03836365 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 120 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Pittsburgh, which has 1,238 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Preoperative counseling office visit is the first listed.
NCT03836365 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT03836365 about?
NCT03836365 is a clinical study titled "Patient Preparedness for Pelvic Organ Prolapse Surgery". Patient preparedness has been associated with increased patient satisfaction, decreased postoperative pain and decreased postoperative narcotic use; however, little is known regarding the optimal way to prepare patients prior to pelvic reconstructive surgery. The primary aim of this study is to dete...
What is the current status of trial NCT03836365?
This trial is currently completed. It is a NA study. The enrollment target is 120 participants. The study started on 2019-04-02. Estimated completion is 2020-05-01.
What interventions are being tested in trial NCT03836365?
The interventions under investigation include: Preoperative counseling office visit (OTHER), Preoperative counseling phone call (OTHER).
Who is sponsoring clinical trial NCT03836365?
This trial is sponsored by University of Pittsburgh, which has 1,238 total clinical trials registered on ClinicalTrials.gov.
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