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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00725907
Other study ID # 6000
Secondary ID MeirMc07om0091CT
Status Completed
Phase N/A
First received July 29, 2008
Last updated July 10, 2011
Start date January 2008
Est. completion date January 2009

Study information

Verified date July 2011
Source Meir Medical Center
Contact n/a
Is FDA regulated No
Health authority Israel: Israeli Health Ministry Pharmaceutical Administration
Study type Interventional

Clinical Trial Summary

PRP will enhance ATFL tears healing by time and quality.


Recruitment information / eligibility

Status Completed
Enrollment 30
Est. completion date January 2009
Est. primary completion date December 2008
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 30 Years
Eligibility Inclusion Criteria:

- athletes 18-30 years old 1st sprain within 3 days from injury

Exclusion Criteria:

Study Design

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


Related Conditions & MeSH terms


Intervention

Biological:
PGRF
injection of 6cc into injured area
placebo saline
injection of 6cc into injured area

Locations

Country Name City State
Israel Meir Medical 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 time to return to active sport 2 No
See also
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