Clinical Trials Directory

Trials / Completed

CompletedNCT03084536

PECS Block vs. Multimodal Analgesia for Prevention of Persistent Postoperative Pain in Breast Surgery

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
134 (actual)
Sponsor
Washington University School of Medicine · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Not accepted

Summary

In this double blinded randomized placebo-controlled trial, 160 subjects scheduled for breast surgery involving the axilla will be administered a multimodal pain regimen including acetaminophen, dexamethasone, celecoxib, and gabapentin. 80 subjects will also receive a Pectoral Nerve blocks I and II (PECS I and II block) preoperatively.

Conditions

Interventions

TypeNameDescription
DRUGBupivacaine-Given after general anesthesia
DRUGGabapentin* As per routine care * Will not be prescribed for any patient with preexisting kidney disease or ≥ 65 years.
DRUGCelecoxib* As per routine care * Will not be prescribed for any patient with preexisting kidney disease or ≥ 65 years. * Naproxen will be substituted for celecoxib in patients with sulfa allergies.
DRUGAcetaminophen-As per routine care
DRUGMidazolam-As per routine care
DRUGFentanyl-As per routine care

Timeline

Start date
2017-06-07
Primary completion
2021-02-25
Completion
2021-02-25
First posted
2017-03-21
Last updated
2024-12-24
Results posted
2022-03-31

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT03084536. Inclusion in this directory is not an endorsement.