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NCT04928339 · ClinicalTrials.gov registry record · Phase 4

Pecto-Intercostal Fascial Plane Block Study

A Phase 4 study, sponsored by University of Wisconsin, Madison.

Completed
Registry status
Phase 4
Development phase
100
Enrollment target

NCT04928339 is a Phase 4 study that has completed, run by University of Wisconsin, Madison. The registered enrollment target is 100 participants.

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The verdict

NCT04928339, a Phase 4 study, has completed, sponsored by University of Wisconsin, Madison.

COMPLETED
Registry status
Phase 4
Development phase
100 participants
Enrollment target

Study Summary

This study is being done to see if bilateral pecto-intercostal fascial plane blocks (PIFB) with a mixture of liposomal and standard bupivacaine decrease pain and opioid requirements in patients undergoing cardiac surgery via median sternotomy compared to controls (sham blocks with saline). 100 participants will be recruited and can expect to be on study for 100 days.

Interventions

  • OTHER Saline
  • DRUG Liposomal bupivacaine
  • DRUG Bupivacaine Injection

Trial Details

FieldValue
Enrollment Target 100 participants
Start Date 2022-03-28
Est. Completion 2023-11-30
Phase Phase 4

Sponsor

University of Wisconsin, Madison

1,039 total trials

What the Registry Record Tells You About NCT04928339

The ClinicalTrials.gov registry entry for NCT04928339 describes a study currently listed as completed, categorized as Phase 4. 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 University of Wisconsin, Madison, which has 1,039 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 3 interventions - of which Saline is the first listed.

NCT04928339 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT04928339 about?

NCT04928339 is a clinical study titled "Pecto-Intercostal Fascial Plane Block Study". This study is being done to see if bilateral pecto-intercostal fascial plane blocks (PIFB) with a mixture of liposomal and standard bupivacaine decrease pain and opioid requirements in patients undergoing cardiac surgery via median sternotomy compared to controls (sham blocks with saline). 100 parti...

What is the current status of trial NCT04928339?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 100 participants. The study started on 2022-03-28. Estimated completion is 2023-11-30.

What interventions are being tested in trial NCT04928339?

The interventions under investigation include: Saline (OTHER), Liposomal bupivacaine (DRUG), Bupivacaine Injection (DRUG).

Who is sponsoring clinical trial NCT04928339?

This trial is sponsored by University of Wisconsin, Madison, which has 1,039 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.