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
| Type | Name | Description |
|---|---|---|
| DRUG | Acetaminophen/Ibuprofen | Postoperatively, subjects will be given acetaminophen 500 mg / ibuprofen 400mg every 4 hours, as needed, for one week or until essentially pain-free |
| DRUG | Acetaminophen/Hydrocodone | Postoperatively, 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.