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NCT05795413 · ClinicalTrials.gov registry record

Quality of Recovery From Mastectomy With and Without PECS Blocks

A clinical trial of Post Operative Pain and Quality of Recovery After Mastectomy, sponsored by Endeavor Health.

Active
Registry status
800
Enrollment target
1
Study location

NCT05795413 is a study of Post Operative Pain and Quality of Recovery After Mastectomy that is active but no longer recruiting, run by Endeavor Health. The registered enrollment target is 800 participants, above the 222-participant average among 56 other Post Operative Pain trials with a reported enrollment target (260% higher). The trial reports 1 study location across 1 state.

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The verdict

NCT05795413, a study of Post Operative Pain and Quality of Recovery After Mastectomy, is active but no longer recruiting, sponsored by Endeavor Health.

ACTIVE NOT RECRUITING
Registry status
800 participants
Enrollment target
1
Study location

Study Summary

This is a prospective observational study. Investigators want to understand post-operative recovery for patients undergoing mastectomy at NorthShore University HealthSystem. Some of these patients receive PECS blocks with Liposomal Bupivacaine and some do not receive a block. Investigators want to know whether patients who receive a block have better post operative recovery and pain control than patients who do not receive one. Investigators also want to understand whether PECS blocks with Liposomal Bupivacaine improves quality of recovery at 72 hours post operatively.

Conditions Studied

Post Operative Pain Quality of Recovery After Mastectomy

Interventions

  • DRUG Liposomal bupivacaine
  • PROCEDURE Mastectomy with PECS blocks

Study Locations (1)

Illinois

  • Evanston Hospital - Evanston

Trial Details

FieldValue
Enrollment Target 800 participants
Start Date 2023-04-25
Est. Completion 2027-04

Sponsor

Endeavor Health

94 total trials

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What the Registry Record Tells You About NCT05795413

The ClinicalTrials.gov registry entry for NCT05795413 describes a study currently listed as active not recruiting, categorized as an unspecified phase. The registered enrollment target is 800 participants, a figure that helps gauge the scale of data the investigators plan to collect, above the 222-participant average among 56 other Post Operative Pain trials with a reported enrollment target (260% higher). The listed sponsor is Endeavor Health, which has 94 total studies on file at ClinicalTrials.gov.

The record links to 2 conditions, with Post Operative Pain appearing as the primary indexed condition, and to 2 interventions - of which Liposomal bupivacaine is the first listed.

NCT05795413 reports 1 study location spanning 1 distinct geographic area - top geographies include Illinois.

Frequently Asked Questions

What is clinical trial NCT05795413 about?

NCT05795413 is a clinical study titled "Quality of Recovery From Mastectomy With and Without PECS Blocks". This is a prospective observational study. Investigators want to understand post-operative recovery for patients undergoing mastectomy at NorthShore University HealthSystem. Some of these patients receive PECS blocks with Liposomal Bupivacaine and some do not receive a block. Investigators want to k...

What is the current status of trial NCT05795413?

This trial is currently active not recruiting. The enrollment target is 800 participants. The study started on 2023-04-25. Estimated completion is 2027-04.

What conditions does trial NCT05795413 study?

This clinical trial studies the following conditions: Post Operative Pain, Quality of Recovery After Mastectomy.

What interventions are being tested in trial NCT05795413?

The interventions under investigation include: Liposomal bupivacaine (DRUG), Mastectomy with PECS blocks (PROCEDURE).

Who is sponsoring clinical trial NCT05795413?

This trial is sponsored by Endeavor Health, which has 94 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05795413 being conducted?

This trial has 1 study location across Illinois. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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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.