Regional Anesthesia Military Battlefield Pain Outcomes Study

CompletedOBSERVATIONAL
Enrollment

386

Participants

Timeline

Start Date

October 31, 2007

Primary Completion Date

September 30, 2013

Study Completion Date

November 30, 2014

Conditions
Anxiety DisordersComplex Regional Pain Syndrome Type IIDepressive DisordersPost-Traumatic Stress DisorderSubstance Abuse
Interventions
PROCEDURE

Regional Anesthesia

Subject received regional anesthesia to affected limb(s) within 72 hours of traumatic event.

PROCEDURE

Standard Pain Management Protocol

Intermittent dosing of analgesics and anxiolytics instituted prior to continuous intravenously dosing which was individually titrated to patient care goals.

Trial Locations (3)

19104

Pain Management Service, Philadelphia

20889

Walter Reed National Military Medical Center, Bethesda

78234

Brooke Army Medical Center & US Army Institute of Surgical Research, Fort Sam Houston

All Listed Sponsors
collaborator

Walter Reed National Military Medical Center

FED

collaborator

Brooke Army Medical Center

FED

collaborator

University of Pennsylvania

OTHER

lead

VA Office of Research and Development

FED

NCT00431847 - Regional Anesthesia Military Battlefield Pain Outcomes Study | Biotech Hunter | Biotech Hunter