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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 is a Phase 4 study that was terminated before completion, run by University of Louisville. The registered enrollment target is 75 participants.

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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.

Interventions

  • DRUG Depodur
  • PROCEDURE sciatic nerve block

Trial Details

FieldValue
Enrollment Target 75 participants
Start Date 2009-12
Est. Completion 2012-12
Phase Phase 4

Sponsor

University of Louisville

217 total trials

What the Registry Record Tells You About NCT00895531

The ClinicalTrials.gov registry entry for NCT00895531 describes a study currently listed as terminated, categorized as Phase 4. The registered enrollment target is 75 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Louisville, which has 217 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which Depodur is the first listed.

NCT00895531 reports 0 study locations.

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.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

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.