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NCT00895531 · ClinicalTrials.gov registry record · Phase 4
Combination of Peripheral Nerve Block and DepoDur in Total Knee Joint Replacement
A Phase 4 study, sponsored by University of Louisville.
- Terminated
- Registry status
- Phase 4
- Development phase
- 75
- Enrollment target
NCT00895531: Clinical Trial Phase 4 study, sponsored by University of Louisville.
NCT00895531 is a Phase 4 study that was terminated before completion, run by University of Louisville. The registered enrollment target is 75 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (86% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00895531, a Phase 4 study, was terminated before completion, sponsored by University of Louisville.
- TERMINATED
- Registry status
- Phase 4
- Development phase
- 75 participants
- Enrollment target
Study Summary
The investigators hypothesize that patients who receive a femoral catheter with low dose epidural Depodur will experience comparable or superior pain relief than those who receive both femoral and sciatic catheters. In addition, the investigators hypothesize that the one catheter will be less time consuming to place and facilitate early ambulation of the patient.
Primary Outcome
Pain as reported on a verbal rating scale ( VRS) (0-10, 0 = no pain, 10 = worse pain imaginable).
Interventions
- DRUG Depodur
- PROCEDURE sciatic nerve block
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 75 participants |
| Start Date | 2009-12 |
| Est. Completion | 2012-12 |
| Phase | Phase 4 |
Why NCT00895531 stopped before completion
NCT00895531 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 75 participants, a relatively small participant target, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (86% lower).
The record links to 0 conditions, and to 2 interventions - of which Depodur is the first listed.
NCT00895531 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00895531 about?
NCT00895531 is a clinical study titled "Combination of Peripheral Nerve Block and DepoDur in Total Knee Joint Replacement". The investigators hypothesize that patients who receive a femoral catheter with low dose epidural Depodur will experience comparable or superior pain relief than those who receive both femoral and sciatic catheters. In addition, the investigators hypothesize that the one catheter will be less time c...
What is the current status of trial NCT00895531?
This trial is currently terminated. It is a Phase 4 study. The enrollment target is 75 participants. The study started on 2009-12. Estimated completion is 2012-12.
What interventions are being tested in trial NCT00895531?
The interventions under investigation include: Depodur (DRUG), sciatic nerve block (PROCEDURE).
Who is sponsoring clinical trial NCT00895531?
This trial is sponsored by University of Louisville, which has 217 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00895531's enrollment target sits among peer trials
75 1002nd of 2000 higher than 974 of 2,000 other Phase 4 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 4 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
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