MAST Trial: Multi-modal Analgesic Strategies in Trauma

NCT03472469 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 1561

Last updated 2021-06-18

Study results available
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Summary

This is a comparative effectiveness study of current pain management strategies in acutely injured trauma patients. Two different multi-modal, opioid minimizing analgesic strategies will be compared \[original multimodal pain regimen (MMPR) compared to multi-modal analgesic strategies for trauma (MAST) MMPR\].

Conditions

  • Nonspecific Pain Post Traumatic Injury

Interventions

DRUG

Acetaminophen IV/PO

Acetaminophen 1g IV/PO every 6 hours

DRUG

Acetaminophen PO

Acetaminophen 1g PO every 6 hours

DRUG

Ketorolac

Ketorolac 30mg IV once

DRUG

Celebrex

Celebrex 200mg PO every 12 hours

DRUG

Naproxen

Naproxen 500mg PO every 12 hours

DRUG

Tramadol

Tramadol 100mg PO every 6 hours

DRUG

Pregabalin

Pregabalin 100mg PO every 8 hours

DRUG

Gabapentin

Gabapentin 300mg PO every 8 hours

DRUG

Lidocaine

Lidocaine patch every 12 hours

DRUG

Opioids

Opioid options include: Oral Opioids (Codeine, Tramadol, Hydrocodone, Oxycodone, Methadone, Morphine, Hydromorphone); Transdermal Opioid (Fentanyl); Intravenous Opioids (Morphine, Hydromorphone, Fentanyl)

DRUG

Regional anesthesia

Regional anesthesia

Sponsors & Collaborators

  • National Center for Advancing Translational Sciences (NCATS)

    collaborator NIH
  • The University of Texas Health Science Center, Houston

    lead OTHER

Principal Investigators

  • John Harvin, MD · The University of Texas Health Science Center, Houston

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
16 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-04-02
Primary Completion
2019-07-03
Completion
2019-07-03
FDA Drug
Yes

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03472469 on ClinicalTrials.gov