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Clinical Trial Summary

The proposed research is to examine the effect of injecting a large volume of HA (10cc) at the time of post arthroscopy suture removal (9-11 day post surgery), in patients with cartilage damage of ICRS grade 2 and above in one of the knee compartments.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT01442571
Study type Interventional
Source Hadassah Medical Organization
Contact Hadas Lemberg, PhD
Phone 00 972 2 6777572
Email lhadas@hadassah.org.il
Status Not yet recruiting
Phase Phase 1/Phase 2

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