Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT01571492 · ClinicalTrials.gov registry record · NA
Continuous L2 Paravertebral Block Versus Continuous Lumbar Plexus Block for Postoperative Analgesia
A NA study of Total Hip Arthroplasty, sponsored by University of Pittsburgh.
- Completed
- Registry status
- NA
- Development phase
- 60
- Enrollment target
- 1
- Study location
NCT01571492 is a NA study of Total Hip Arthroplasty that has completed, run by University of Pittsburgh. The registered enrollment target is 60 participants, below the 140-participant average among 12 other Total Hip Arthroplasty trials with a reported enrollment target (57% lower). The trial reports 1 study location across 1 state.
The verdict
NCT01571492, a NA study of Total Hip Arthroplasty, has completed, sponsored by University of Pittsburgh.
- COMPLETED
- Registry status
- NA
- Development phase
- 60 participants
- Enrollment target
- 1
- Study location
Study Summary
This prospective study is intended to compare the analgesic efficacy, preservation of lower extremity motor power and side-effect profile of L2 Paravertebral lumbar plexus approach compared to Posterior nerve stimulation guided lumbar plexus approach, continuous local anesthetic infusion postoperative analgesia of Total Hip Arthroplasty. The L2 Paravertebral technique of lumbar plexus block, as part of a multimodal pain treatment, could be a cost-effective alternative with a equal profile of analgesic efficacy and motor power sparing with greater promotion of early achievement of postoperative physical therapy goals.
Conditions Studied
Interventions
- PROCEDURE L2 Paravertebral catheter nerve block
- PROCEDURE Continuous Lumbar plexus nerve block
Study Locations (1)
Pennsylvania
- UPMC Presbyterian Shadyside - Pittsburgh
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 60 participants |
| Start Date | 2009-06 |
| Est. Completion | 2015-06 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01571492
The ClinicalTrials.gov registry entry for NCT01571492 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 60 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 140-participant average among 12 other Total Hip Arthroplasty trials with a reported enrollment target (57% lower). The listed sponsor is University of Pittsburgh, which has 1,238 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Total Hip Arthroplasty appearing as the primary indexed condition, and to 2 interventions - of which L2 Paravertebral catheter nerve block is the first listed.
NCT01571492 reports 1 study location spanning 1 distinct geographic area - top geographies include Pennsylvania.
Frequently Asked Questions
What is clinical trial NCT01571492 about?
NCT01571492 is a clinical study titled "Continuous L2 Paravertebral Block Versus Continuous Lumbar Plexus Block for Postoperative Analgesia". This prospective study is intended to compare the analgesic efficacy, preservation of lower extremity motor power and side-effect profile of L2 Paravertebral lumbar plexus approach compared to Posterior nerve stimulation guided lumbar plexus approach, continuous local anesthetic infusion postoperati...
What is the current status of trial NCT01571492?
This trial is currently completed. It is a NA study. The enrollment target is 60 participants. The study started on 2009-06. Estimated completion is 2015-06.
What conditions does trial NCT01571492 study?
This clinical trial studies the following conditions: Total Hip Arthroplasty.
What interventions are being tested in trial NCT01571492?
The interventions under investigation include: L2 Paravertebral catheter nerve block (PROCEDURE), Continuous Lumbar plexus nerve block (PROCEDURE).
Who is sponsoring clinical trial NCT01571492?
This trial is sponsored by University of Pittsburgh, which has 1,238 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT01571492 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 Total Hip Arthroplasty
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.
-
G7 Acetabular System With Vivacit-E or Longevity Liner PMCF Study
RECRUITING · NA
-
Patient Utilization of Opioid Destruction Bags in the Post-op Period
ACTIVE NOT RECRUITING · NA
-
Strength and Function Following Total Hip Arthroplasty
COMPLETED · NA
-
Improving Rehabilitation Outcomes After Total Hip Arthroplasty
COMPLETED · NA
-
Anterior Capsulectomy vs. Repair in Direct Anterior THA
COMPLETED · NA
-
The Effect of Tranexamic Acid on Blood Coagulation in Total Hip Arthroplasty Surgery
COMPLETED · NA
Read our methodology - how this data is sourced, computed, and verified.
Related
Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.