MAST Trial: Multi-modal Analgesic Strategies in Trauma
NCT03472469 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 1561
Last updated 2021-06-18
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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