Clinical Trials Directory

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

TypeNameDescription
DRUGKetorolacthe investigators aimed to evaluate the effect of postoperative ketorolac after ankle fracture surgery on postoperative opioid consumption, pain control, an patient satisfaction.
OTHERNo ketorolacstandard 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

Source: ClinicalTrials.gov record NCT03727048. Inclusion in this directory is not an endorsement.