Comparison of Efficacy and Safety of Microfracture and Modified Microfracture

NCT02539030 · Status: UNKNOWN · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 100

Last updated 2015-09-02

No results posted yet for this study

Summary

This study was designed to evaluate the efficacy and safety of a modified microfracture using collagen, and to compare them with those of a simple microfracture to prove the non-inferiority of the modified microfracture using collagen in patients with cartilage defects in their knees.

Conditions

Interventions

PROCEDURE

Microfracture

simple microfracture

DEVICE

CartiFill

add collagen when doing microfracture

Sponsors & Collaborators

  • Sewon Cellontech Co., Ltd.

    lead INDUSTRY

Principal Investigators

  • Nam Yong Choi, MD · Catholic University of Korea Saint Paul's Hospital

  • Yong In, MD · The Catholic University of Korea

  • Chan Woong Moon, MD · The Catholic University of Korea Bucheon St.Mary's Hospital

  • Hae Seock Ko, MD · The Catholic University of Korea Vincent's Hospital

  • Cheol Hong Jeon, MD · Wonkwang University Hospital

  • Seung Back Kang, MD · SMG-SNU Boramae Medical Center

  • Ja Young Choi, MD · Seoul National University Hospital

  • Myung Koo Kim, MD · Inha University Hospital

  • Jae Kyun Jun, MD · Daejeon Sun hospital

  • Jae Doo Yoo, MD · Ewha Womans University Mokdong Hospital

  • Jung Koo Ha, MD · Inje University

  • Jun Ho Wang, MD · Samsung Medical Center

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
15 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2013-02-28
Primary Completion
2016-01-31
Completion
2017-06-30

Countries

  • South Korea

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02539030 on ClinicalTrials.gov