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NCT04910165 · ClinicalTrials.gov registry record · Phase 3

Exparel Use in Adductor Canal Block After Total Knee Arthroplasty

A Phase 3 study, sponsored by St. Luke's Hospital, Pennsylvania.

Completed
Registry status
Phase 3
Development phase
100
Enrollment target

NCT04910165 is a Phase 3 study that has completed, run by St. Luke's Hospital, Pennsylvania. The registered enrollment target is 100 participants.

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The verdict

NCT04910165, a Phase 3 study, has completed, sponsored by St. Luke's Hospital, Pennsylvania.

COMPLETED
Registry status
Phase 3
Development phase
100 participants
Enrollment target

Study Summary

Exparel has been shown to have better pain control compared to previously used infiltration agents, including bupivacaine, while having a minor side effect profile. The purpose of this study is to explore the effectiveness of Exparel (liposomal bupivacaine) in Adductor Canal Blocks for peri-operative pain control following a total knee arthroplasty (TKA) procedure.

Interventions

  • DRUG Exparel
  • DRUG Ropivacaine

Trial Details

FieldValue
Enrollment Target 100 participants
Start Date 2020-06-01
Est. Completion 2021-10-15
Phase Phase 3

Sponsor

St. Luke's Hospital, Pennsylvania

10 total trials

What the Registry Record Tells You About NCT04910165

The ClinicalTrials.gov registry entry for NCT04910165 describes a study currently listed as completed, categorized as Phase 3. The registered enrollment target is 100 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is St. Luke's Hospital, Pennsylvania, which has 10 total studies on file at ClinicalTrials.gov.

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

NCT04910165 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT04910165 about?

NCT04910165 is a clinical study titled "Exparel Use in Adductor Canal Block After Total Knee Arthroplasty". Exparel has been shown to have better pain control compared to previously used infiltration agents, including bupivacaine, while having a minor side effect profile. The purpose of this study is to explore the effectiveness of Exparel (liposomal bupivacaine) in Adductor Canal Blocks for peri-operativ...

What is the current status of trial NCT04910165?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 100 participants. The study started on 2020-06-01. Estimated completion is 2021-10-15.

What interventions are being tested in trial NCT04910165?

The interventions under investigation include: Exparel (DRUG), Ropivacaine (DRUG).

Who is sponsoring clinical trial NCT04910165?

This trial is sponsored by St. Luke's Hospital, Pennsylvania, which has 10 total clinical trials registered on ClinicalTrials.gov.

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

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.