Clinical Trials Logo

Clinical Trial Summary

This is a single-center, randomized, single-blind (evaluator) study. Enrolled patients had a traumatic meniscal tear and underwent meniscectomy. The study included 6 weeks (12 visits) of standard or quadriceps intensive rehabilitation. The objective of the study was to determine the effect of quadriceps intensive rehabilitation on knee function and articular cartilage.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT01879852
Study type Interventional
Source University of Florida
Contact
Status Completed
Phase N/A
Start date October 2008
Completion date August 2013

See also
  Status Clinical Trial Phase
Terminated NCT03696836 - AIR (Artificial Implant for Medial Meniscus Replacement) Study N/A
Completed NCT04644640 - Telerehabilitation Following Meniscectomy N/A
Recruiting NCT04972331 - Degenerative Meniscus Without Osteoarthritis : Arthroscopic Partial Menisectomy Versus Platelet Rich Plasma (APM-PRP) N/A
Completed NCT03350204 - Biomechanical Osteoarthritis Outcomes in Meniscectomy Patients N/A
Completed NCT02181426 - Dose Response of Ketorolac in Knee Arthroscopy N/A
Completed NCT02136901 - The VENUS Clinical Study (Verifying the Effectiveness of the NUsurface® System) N/A
Completed NCT02108496 - Verifying the Effectiveness of the NUsurface® System N/A
Completed NCT01158677 - Short Term Outcome After Meniscectomy
Completed NCT02872753 - Intra-operative Injection of Autologous Conditioned Plasma (ACP) Following Partial Meniscectomy Phase 4
Enrolling by invitation NCT04717609 - Saphenous Nerve Block for Partial Meniscectomy Phase 3
Completed NCT01571102 - Impact of Physiotherapy on Short-term Outcome After Meniscectomy N/A
Terminated NCT00314457 - Efficacy Study of Continuous Intraarticular Infusion in Patients Undergoing Arthroscopic Knee and Shoulder Operations Phase 4