Trials / Completed
CompletedNCT03727048
Effect of Toradol on Post-operative Foot and Ankle Healing
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 128 (actual)
- Sponsor
- Rothman Institute Orthopaedics · Academic / Other
- Sex
- All
- Age
- 18 Years – 100 Years
- Healthy volunteers
- Not accepted
Summary
The use of Toradol for pain control in surgical orthopedic cases is currently a topic of interest within the field. The proposed study is a prospective randomized study evaluating postoperative pain, opioid requirement, complication/reoperation rates and nonunion rates in patients undergoing surgical treatment for isolated lateral malleolar fibula fractures. Patients will be randomized to either the Treatment Group (Toradol) or the Control Group (Non-Toradol). Both Toradol and non-Toradol drug regimens are currently prescribed by the Foot and Ankle Team at the Rothman Institute and this study will serve as a valuable comparison.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Ketorolac | the investigators aimed to evaluate the effect of postoperative ketorolac after ankle fracture surgery on postoperative opioid consumption, pain control, an patient satisfaction. |
| OTHER | No ketorolac | standard of care post operative pain management protocol |
Timeline
- Start date
- 2016-08-01
- Primary completion
- 2018-03-01
- Completion
- 2018-03-01
- First posted
- 2018-11-01
- Last updated
- 2018-11-01
Regulatory
- FDA-regulated drug study
Source: ClinicalTrials.gov record NCT03727048. Inclusion in this directory is not an endorsement.