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NCT04198714 · ClinicalTrials.gov registry record · NA
Pudendal Nerve Block in Vaginal Surgery
A NA study of Surgery and Pain, Postoperative, sponsored by MetroHealth Medical Center.
- Completed
- Registry status
- NA
- Development phase
- 72
- Enrollment target
- 1
- Study location
NCT04198714 is a NA study of Surgery and Pain, Postoperative that has completed, run by MetroHealth Medical Center. The registered enrollment target is 72 participants, below the 52,851-participant average among 120 other Surgery trials with a reported enrollment target (100% lower). The trial reports 1 study location across 1 state.
The verdict
NCT04198714, a NA study of Surgery and Pain, Postoperative, has completed, sponsored by MetroHealth Medical Center.
- COMPLETED
- Registry status
- NA
- Development phase
- 72 participants
- Enrollment target
- 1
- Study location
Study Summary
The objective of this this randomized controlled study is to determine whether a pudendal nerve block at the time of vaginal surgery is associated with improved postoperative pain control and decrease opioid consumption compared to a sham pudendal nerve block in patients undergoing vaginal surgery.
Conditions Studied
Interventions
- PROCEDURE Pudendal block
Study Locations (1)
Ohio
- MetroHealth Medical Center - Cleveland
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 72 participants |
| Start Date | 2019-08-01 |
| Est. Completion | 2021-09-13 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT04198714
The ClinicalTrials.gov registry entry for NCT04198714 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 72 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 52,851-participant average among 120 other Surgery trials with a reported enrollment target (100% lower). The listed sponsor is MetroHealth Medical Center, which has 76 total studies on file at ClinicalTrials.gov.
The record links to 6 conditions, with Surgery appearing as the primary indexed condition, and to 1 intervention - of which Pudendal block is the first listed.
NCT04198714 reports 1 study location spanning 1 distinct geographic area - top geographies include Ohio.
Frequently Asked Questions
What is clinical trial NCT04198714 about?
NCT04198714 is a clinical study titled "Pudendal Nerve Block in Vaginal Surgery". The objective of this this randomized controlled study is to determine whether a pudendal nerve block at the time of vaginal surgery is associated with improved postoperative pain control and decrease opioid consumption compared to a sham pudendal nerve block in patients undergoing vaginal surgery.
What is the current status of trial NCT04198714?
This trial is currently completed. It is a NA study. The enrollment target is 72 participants. The study started on 2019-08-01. Estimated completion is 2021-09-13.
What conditions does trial NCT04198714 study?
This clinical trial studies the following conditions: Surgery, Pain, Postoperative, Pelvic Organ Prolapse, Pelvic Floor Disorders, Nerve Block.
What interventions are being tested in trial NCT04198714?
The interventions under investigation include: Pudendal block (PROCEDURE).
Who is sponsoring clinical trial NCT04198714?
This trial is sponsored by MetroHealth Medical Center, which has 76 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT04198714 being conducted?
This trial has 1 study location across Ohio. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Related
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