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NCT05795413 · ClinicalTrials.gov registry record
Quality of Recovery From Mastectomy With and Without PECS Blocks
A clinical trial of Postoperative Pain and Quality of Recovery After Mastectomy, sponsored by Endeavor Health.
- Active
- Registry status
- 800
- Enrollment target
- 1
- Study location
NCT05795413: Active study of Postoperative Pain and Quality of Recovery After Mastectomy, sponsored by Endeavor Health.
NCT05795413 is a study of Postoperative 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 225-participant average among 120 other Postoperative Pain trials with a reported enrollment target (256% higher). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT05795413, a study of Postoperative 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.
Primary Outcome
Patients will complete the quality of recovery 15 survey 72 hours after surgery. This is a scale from 0 to 150. A score of 150 indicates better post operative recovery.
Conditions Studied
Interventions
- DRUG Liposomal bupivacaine
- PROCEDURE Mastectomy with PECS blocks
Study Locations (1)
Illinois
- Evanston Hospital - Evanston
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 800 participants |
| Start Date | 2023-04-25 |
| Est. Completion | 2027-04 |
What the registry record for NCT05795413 still lists
NCT05795413 is an observational study that tracks outcomes without assigning an intervention. The registered 800 participants enrollment target is mid-sized for trials with a published cap, above the 225-participant average among 120 other Postoperative Pain trials with a reported enrollment target (256% higher).
The record links to 2 conditions, with Postoperative Pain appearing as the primary indexed condition, and to 2 interventions - of which Liposomal bupivacaine is the first listed.
NCT05795413 reports a single indexed study location in 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: Postoperative 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.
Learn More About Clinical Trials
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Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
Where NCT05795413's enrollment target sits among peer trials
800 7th of 120 higher than 113 of 120 other Postoperative Pain trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Postoperative Pain trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
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