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NCT04508504 · ClinicalTrials.gov registry record · NA
PENG Block for Arthroscopic Hip Surgery
A NA study of Postoperative Pain and Hip Arthroscopy, sponsored by University of Virginia.
- Completed
- Registry status
- NA
- Development phase
- 70
- Enrollment target
- 1
- Study location
NCT04508504 is a NA study of Postoperative Pain and Hip Arthroscopy that has completed, run by University of Virginia. The registered enrollment target is 70 participants, below the 230-participant average among 63 other Postoperative Pain trials with a reported enrollment target (70% lower). The trial reports 1 study location across 1 state.
The verdict
NCT04508504, a NA study of Postoperative Pain and Hip Arthroscopy, has completed, sponsored by University of Virginia.
- COMPLETED
- Registry status
- NA
- Development phase
- 70 participants
- Enrollment target
- 1
- Study location
Study Summary
This randomized, double-blinded, placebo-controlled trial seeks to evaluate the analgesic efficacy of the pericapsular nerve group block in the setting of outpatient hip arthroscopy.
Conditions Studied
Interventions
- DRUG Ropivacaine 0.5% Injectable Solution
- DRUG Normal Saline
- PROCEDURE Preop PENG block
- PROCEDURE Placebo block
Study Locations (1)
Virginia
- UVA Outpatient Surgery Center - Charlottesville
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 70 participants |
| Start Date | 2020-12-01 |
| Est. Completion | 2022-02-08 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT04508504
The ClinicalTrials.gov registry entry for NCT04508504 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 70 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 230-participant average among 63 other Postoperative Pain trials with a reported enrollment target (70% lower). The listed sponsor is University of Virginia, which has 449 total studies on file at ClinicalTrials.gov.
The record links to 2 conditions, with Postoperative Pain appearing as the primary indexed condition, and to 4 interventions - of which Ropivacaine 0.5% Injectable Solution is the first listed.
NCT04508504 reports 1 study location spanning 1 distinct geographic area - top geographies include Virginia.
Frequently Asked Questions
What is clinical trial NCT04508504 about?
NCT04508504 is a clinical study titled "PENG Block for Arthroscopic Hip Surgery". This randomized, double-blinded, placebo-controlled trial seeks to evaluate the analgesic efficacy of the pericapsular nerve group block in the setting of outpatient hip arthroscopy.
What is the current status of trial NCT04508504?
This trial is currently completed. It is a NA study. The enrollment target is 70 participants. The study started on 2020-12-01. Estimated completion is 2022-02-08.
What conditions does trial NCT04508504 study?
This clinical trial studies the following conditions: Postoperative Pain, Hip Arthroscopy.
What interventions are being tested in trial NCT04508504?
The interventions under investigation include: Ropivacaine 0.5% Injectable Solution (DRUG), Normal Saline (DRUG), Preop PENG block (PROCEDURE), Placebo block (PROCEDURE).
Who is sponsoring clinical trial NCT04508504?
This trial is sponsored by University of Virginia, which has 449 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT04508504 being conducted?
This trial has 1 study location across Virginia. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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