Gabapentin And Breast Surgery Decision Architecture Randomization Trial (GABS-DART) Protocol

Recruiting Phase 4 Interventional Study
Breast Cancer
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Prior Safety Data This treatment has already been tested in at least one earlier human trial.
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At a Glance
Age
18 – 65
Sex
Any
Trial phase
Phase 4
Study type
Interventional
Purpose
Treatment
Participants needed
1,896 (estimated)
Sponsor
Memorial Sloan Kettering Cancer Center · Other
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About This Trial

This study aims to assess whether gabapentin should be a standard component of peri-operative pain control in mastectomy patients at Memorial Sloan Kettering Cancer Center.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Age 18 to 65 years * Undergoing ambulatory extended recover (AXR) mastectomy (bilateral or unilateral) at the Josie Robertson Surgical Center (JSRC) Exclusion Criteria: * None
Contacts

James Flory, MD

646-608-2914

floryj@mskcc.org

CONTACT

Andrew Vickers, PhD

646-227-3678

vickersa@MSKCC.ORG

CONTACT