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NCT06574022 · ClinicalTrials.gov registry record · Phase 4

Post-mastectomy Recovery: Comparing Preoperative PECS-II Blocks With Intraoperative Pectoral Blocks

A Phase 4 study of Breast Cancer and Mastectomy; Lymphedema, sponsored by University of Cincinnati.

Recruiting
Registry status
Phase 4
Development phase
100
Enrollment target
1
Study location

NCT06574022 is a Phase 4 study of Breast Cancer and Mastectomy; Lymphedema that is actively recruiting participants, run by University of Cincinnati. The registered enrollment target is 100 participants, below the 2,803-participant average among 1,224 other Breast Cancer trials with a reported enrollment target (96% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT06574022, a Phase 4 study of Breast Cancer and Mastectomy; Lymphedema, is actively recruiting participants, sponsored by University of Cincinnati.

RECRUITING
Registry status
Phase 4
Development phase
100 participants
Enrollment target
1
Study location

Study Summary

The purpose this research is to compare two different standards of care for pain management and two different standards of care for local numbing medicine for breast cancer patients who will have a total mastectomy.

Interventions

  • DRUG Bupivacain
  • DRUG Exparel
  • PROCEDURE Intraoperative Pecs II block (IOB) & superior AT (EX or BP)
  • PROCEDURE Preoperative Pecs II block (POB) & superior AT (EX or BP)

Study Locations (1)

Ohio

  • University of Cincinnati Medical Center - Cincinnati

Trial Details

FieldValue
Enrollment Target 100 participants
Start Date 2024-09-25
Est. Completion 2026-12-01
Phase Phase 4

Sponsor

University of Cincinnati

245 total trials

What the Registry Record Tells You About NCT06574022

The ClinicalTrials.gov registry entry for NCT06574022 describes a study currently listed as recruiting, 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, below the 2,803-participant average among 1,224 other Breast Cancer trials with a reported enrollment target (96% lower). The listed sponsor is University of Cincinnati, which has 245 total studies on file at ClinicalTrials.gov.

The record links to 2 conditions, with Breast Cancer appearing as the primary indexed condition, and to 4 interventions - of which Bupivacain is the first listed.

NCT06574022 reports 1 study location spanning 1 distinct geographic area - top geographies include Ohio.

Frequently Asked Questions

What is clinical trial NCT06574022 about?

NCT06574022 is a clinical study titled "Post-mastectomy Recovery: Comparing Preoperative PECS-II Blocks With Intraoperative Pectoral Blocks". The purpose this research is to compare two different standards of care for pain management and two different standards of care for local numbing medicine for breast cancer patients who will have a total mastectomy.

What is the current status of trial NCT06574022?

This trial is currently recruiting. It is a Phase 4 study. The enrollment target is 100 participants. The study started on 2024-09-25. Estimated completion is 2026-12-01.

What conditions does trial NCT06574022 study?

This clinical trial studies the following conditions: Breast Cancer, Mastectomy; Lymphedema.

What interventions are being tested in trial NCT06574022?

The interventions under investigation include: Bupivacain (DRUG), Exparel (DRUG), Intraoperative Pecs II block (IOB) & superior AT (EX or BP) (PROCEDURE), Preoperative Pecs II block (POB) & superior AT (EX or BP) (PROCEDURE).

Who is sponsoring clinical trial NCT06574022?

This trial is sponsored by University of Cincinnati, which has 245 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06574022 being conducted?

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

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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.