drugset / Trial / NCT02263222

A Feasibility Dose-escalating Study of MDT-10013 for Acute Postoperative Pain Following Total Knee Arthroplasty

NCT02263222 ↗

Phase 2 Withdrawn Medtronic Spinal and Biologics
NaSingle-groupOpen-labelTreatment

Summary

This is an open-label dose-escalating study to evaluate the tolerability and systemic exposure of MDT-10013 in men and women at least 18 years of age who are undergoing primary unilateral TKA.

Timeline

Start
2016-02
Primary completion
2016-06
Completion
2016-06

Drugs

EvaluationDrugModalityDoseRoute
Subject MDT-10013 Unknown — —

Indications

No indication recorded.