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NCT02882633 · ClinicalTrials.gov registry record · NA
Lumbar Plexus Block vs Fascia Iliaca Block After Hip Arthroscopy
A NA study of Hip Arthroscopy and Nerve Block, sponsored by University of Pennsylvania.
- Completed
- Registry status
- NA
- Development phase
- 50
- Enrollment target
- 1
- Study location
NCT02882633: Completed NA study of Hip Arthroscopy and Nerve Block, sponsored by University of Pennsylvania.
NCT02882633 is a NA study of Hip Arthroscopy and Nerve Block that has completed, run by University of Pennsylvania. The registered enrollment target is 50 participants, below the 1,122-participant average among 10 other Hip Arthroscopy trials with a reported enrollment target (96% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT02882633, a NA study of Hip Arthroscopy and Nerve Block, has completed, sponsored by University of Pennsylvania.
- COMPLETED
- Registry status
- NA
- Development phase
- 50 participants
- Enrollment target
- 1
- Study location
Study Summary
The purpose of this study is to compare lumbar plexus block to fascia iliac block done in adult patients who have undergone hip arthroscopy surgery. Visual analogue scores, opioid consumption, and quality of recovery 48 hours post operatively will be used for comparison.
Primary Outcome
Change in pain scores, as measured by the Visual Analog Scale (0-10). 10 is worst imaginable pain and 0 means no pain at all.
Conditions Studied
Interventions
- DRUG 30ml bolus of bupivacaine
Study Locations (1)
Pennsylvania
- University of Pennsylvania - Philadelphia
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 50 participants |
| Start Date | 2015-11 |
| Est. Completion | 2018-05 |
| Phase | NA |
What the finished NCT02882633 record still lists
NCT02882633 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 50 participants, a relatively small participant target, below the 1,122-participant average among 10 other Hip Arthroscopy trials with a reported enrollment target (96% lower).
The record links to 2 conditions, with Hip Arthroscopy appearing as the primary indexed condition, and to 1 intervention - of which 30ml bolus of bupivacaine is the first listed.
NCT02882633 reports a single indexed study location in Pennsylvania.
Frequently Asked Questions
What is clinical trial NCT02882633 about?
NCT02882633 is a clinical study titled "Lumbar Plexus Block vs Fascia Iliaca Block After Hip Arthroscopy". The purpose of this study is to compare lumbar plexus block to fascia iliac block done in adult patients who have undergone hip arthroscopy surgery. Visual analogue scores, opioid consumption, and quality of recovery 48 hours post operatively will be used for comparison.
What is the current status of trial NCT02882633?
This trial is currently completed. It is a NA study. The enrollment target is 50 participants. The study started on 2015-11. Estimated completion is 2018-05.
What conditions does trial NCT02882633 study?
This clinical trial studies the following conditions: Hip Arthroscopy, Nerve Block.
What interventions are being tested in trial NCT02882633?
The interventions under investigation include: 30ml bolus of bupivacaine (DRUG).
Who is sponsoring clinical trial NCT02882633?
This trial is sponsored by University of Pennsylvania, which has 1,423 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT02882633 being conducted?
This trial has 1 study location across Pennsylvania. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Hip Arthroscopy
Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
Where NCT02882633's enrollment target sits among peer trials
50 11th of 10 the lowest of 10 other Hip Arthroscopy trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Hip Arthroscopy trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
-
Absorbable vs Non-Absorbable Sutures for Hip Capsular Closure
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-
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-
Effect of Post-operative Brace on Pain and Patient Outcomes Following Hip Arthroscopy for FAIS
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-
CREST: Capsular Repair During Hip Arthroscopy
ACTIVE NOT RECRUITING · NA
-
Pain Control in Hip Arthroscopy: Comparing Lumbar Plexus Versus Peri-capsular Injection
COMPLETED · NA
-
PENG Block for Arthroscopic Hip Surgery
COMPLETED · NA
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