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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00726245
Other study ID # 3000
Secondary ID
Status Completed
Phase Phase 2/Phase 3
First received July 29, 2008
Last updated July 10, 2011
Start date January 2008
Est. completion date March 2011

Study information

Verified date July 2011
Source Meir Medical Center
Contact n/a
Is FDA regulated No
Health authority Israel: The Israel National Institute for Health Policy Research and Health Services Research
Study type Interventional

Clinical Trial Summary

the improvement of symptoms and disease progress by the treatment of OA of the knee with PRGF


Recruitment information / eligibility

Status Completed
Enrollment 50
Est. completion date March 2011
Est. primary completion date February 2009
Accepts healthy volunteers No
Gender Both
Age group 15 Years to 40 Years
Eligibility Inclusion Criteria:

- US diagnosed muscle tear

- age 15-40 years old

Exclusion Criteria:

- pregnancy

- mental or physical disabilities

Study Design

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


Related Conditions & MeSH terms


Intervention

Biological:
PRGF
3-6mg IM (to area of muscle tear)
Placebo
3cc IM of physiological saline

Locations

Country Name City State
Israel Meir Medicak Center Kfar Saba

Sponsors (1)

Lead Sponsor Collaborator
Meir Medical Center

Country where clinical trial is conducted

Israel, 

Outcome

Type Measure Description Time frame Safety issue
Primary improvement of symptoms / disease progress 1 year Yes
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