Osteochondritis Dissecans of the Knee NCT01455987

Updated 05/31/2024

Clinical Trial Details — Status: Enrolling by invitation

Administrative data
NCT number	NCT01455987
Other study ID #	KUH5203050
Secondary ID
Status	Enrolling by invitation
Phase	N/A
First received	January 4, 2011
Last updated	October 19, 2011
Start date	June 2010
Est. completion date	December 2013

Study information
Verified date	October 2011
Source	Kuopio University Hospital
Contact	n/a
Is FDA regulated	No
Health authority	Finland: Ethics Committee
Study type	Observational

Clinical Trial Summary

Osteochondritis dissecans is a relatively common...

Recruitment information / eligibility
Status	Enrolling by invitation
Enrollment	265
Est. completion date	December 2013
Est. primary completion date	December 2012
Accepts healthy volunteers	No
Gender	Both
Age group	N/A and older
Eligibility	Inclusion Criteria: - Osteochondritis dissecans diagnosis code (ICD-8 to -10) in the medical records of KUH - Knee OCD verified from the medical records Exclusion Criteria: -Any other medical condition

Study Design

Observational Model: Cohort, Time Perspective: Retrospective

Related Conditions & MeSH terms

Juvenile Osteochondritis Dissecans
Osteochondritis
Osteochondritis Dissecans

Locations
Country	Name	City	State
n/a

Sponsors *(1)*
Lead Sponsor	Collaborator
Kuopio University Hospital

Outcome
Type	Measure	Description	Time frame	Safety issue
Primary	Knee pain measured by NRS (numeric rating scale, 0-10)	0=no pain 10=maximal pain	At the time of recruiting, which is an avarage calculated from all participiants enrolled for this study (estimated avarage follow-up 12-16 years).	No
Secondary	Lysholm Knee Score and Knee Injury and Osteoarthritis Outcome Score (KOOS)	Lysholm Knee Score and KOOS are validated subjective questionares assessing outcome after knee surgery/injury.	At the time of recruiting, which is an avarage calculated from all participiants enrolled for this study (estimated avarage follow-up 12-16 years).	No

See also
	Status	Clinical Trial	Phase
	Active, not recruiting	`NCT01458782` - ACI-C Versus AMIC. A Randomized Trial Comparing Two Methods for Repair of Cartilage Defects in the Knee	N/A
	Active, not recruiting	`NCT02771496` - Osteochondritis Dissecans of Knee Prospective Cohort
	Completed	`NCT02397278` - Intra Articular Injections With Platelet Rich Plasma in Patients With Juvenile Osteochondritis Dissecans of the Knee	N/A
	Active, not recruiting	`NCT01347892` - DeNovo NT Ankle LDC Study	N/A
	Recruiting	`NCT01409447` - Repair of Articular Osteochondral Defect	N/A
	Active, not recruiting	`NCT03656185` - Elbow Arthroscopy Data Analysis
	Completed	`NCT01471236` - Evaluation of the Agili-C Biphasic Implant in the Knee Joint	N/A
	Recruiting	`NCT01159899` - Transplantation of Bone Marrow Stem Cells Stimulated by Proteins Scaffold to Heal Defects Articular Cartilage of the Knee	Phase 0
	Terminated	`NCT00881023` - Cartilage Autograft Implantation System (CAIS) for the Repair of Knee Cartilage Through Cartilage Regeneration	N/A
	Recruiting	`NCT04364334` - Knee Registry (Knieregister)
	Recruiting	`NCT01498029` - Knee Articular Cartilage Repair: Cartilage Autograft Implantation System Versus Conventional Microfracture	Phase 3
	Completed	`NCT03452098` - Post-Operative Rehabilitation of Knee Osteochondral Defect: A Case Series
	Completed	`NCT04297449` - Prospective 2-year Data Collection of the First 10 Patients After Ankle Spacer Implantation
	Suspended	`NCT02664337` - Conjoint Analysis of Patient Preferences in Joint Interventions	N/A
	Active, not recruiting	`NCT01329445` - DeNovo NT Longitudinal Data Collection (LDC) Knee Study	N/A
	Completed	`NCT02993510` - A Randomized Controlled Trial Comparing Chondro-Gide® to Microfracture Alone for Treatment of Knee Cartilage Defects.	Phase 3
	Recruiting	`NCT01694823` - Safety and Efficacy Study of Cells Sheet-Autologous Chondrocyte Implantation to Treat Articular Cartilage Defects	Phase 1/Phase 2
	Withdrawn	`NCT01283737` - Use of Demineralised Bone Matrix (DBX) in Osteochondritis Dissecans (OCD)	Phase 4