Clinical Trials Directory

Trials / Terminated

TerminatedNCT02029235

Post-operative Analgesia in Elective, Soft-tissue Hand Surgery

Post-operative Analgesia in Elective, Soft-tissue Hand Surgery: A Randomized, Double Blind Comparison of Acetaminophen/Ibuprofen Versus Acetaminophen/Hydrocodone

Status
Terminated
Phase
Phase 4
Study type
Interventional
Enrollment
72 (actual)
Sponsor
Alexander Payatakes, M.D. · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this research study is to find out which combination of pain medications following surgery work the best and result in the fewest side effects.

Detailed description

This is a prospective, randomized, double-blind study comparing the efficacy of acetaminophen/hydrocodone (AH) to acetaminophen/ibuprofen (AIBU) in providing adequate post-operative pain relief in elective, soft tissue hand surgery patients.

Conditions

Interventions

TypeNameDescription
DRUGAcetaminophen/IbuprofenPostoperatively, subjects will be given acetaminophen 500 mg / ibuprofen 400mg every 4 hours, as needed, for one week or until essentially pain-free
DRUGAcetaminophen/HydrocodonePostoperatively, subjects will be given acetaminophen 325 mg / hydrocodone 5 mg every 4 hours, as needed, for one week or until essentially pain-free

Timeline

Start date
2015-02-10
Primary completion
2017-11-17
Completion
2018-06-30
First posted
2014-01-07
Last updated
2018-12-13
Results posted
2018-12-13

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT02029235. Inclusion in this directory is not an endorsement.