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ACTIVE NOT RECRUITING

Quality of Recovery From Mastectomy With and Without PECS Blocks

NCT05795413 · View on ClinicalTrials.gov ↗

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.

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

115 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT05795413

The ClinicalTrials.gov registry entry for NCT05795413 describes a study currently listed as active not recruiting. It is categorized as an unspecified phase, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 800 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Endeavor Health, which has 115 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

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. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT05795413 reports 1 study location spanning 1 distinct geographic area — top geographies include Illinois. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

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. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT05795413?

The interventions under investigation include: Liposomal bupivacaine (DRUG), Mastectomy with PECS blocks (PROCEDURE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT05795413?

This trial is sponsored by Endeavor Health, which has 115 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

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.

Related

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