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
| Type | Name | Description |
|---|---|---|
| DRUG | Bupivacaine | -Given after general anesthesia |
| DRUG | Gabapentin | * As per routine care * Will not be prescribed for any patient with preexisting kidney disease or ≥ 65 years. |
| DRUG | Celecoxib | * 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. |
| DRUG | Acetaminophen | -As per routine care |
| DRUG | Midazolam | -As per routine care |
| DRUG | Fentanyl | -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
- FDA-regulated drug study
Source: ClinicalTrials.gov record NCT03084536. Inclusion in this directory is not an endorsement.