Pain Relief by Platelet-rich Plasma (PRP) Treatment

This study is ongoing, but not recruiting participants.
Information provided by (Responsible Party):
Saint Bernard Mission University Identifier:
First received: December 11, 2012
Last updated: December 12, 2012
Last verified: December 2012

Past PRP therapy is not sufficient for some part of patients.In this clinical research, The integrated application of PRP with extracellurar matrix and some type of stem cell technique.


Study Type: Observational
Study Design: Observational Model: Case Control
Time Perspective: Prospective

Resource links provided by NLM:

Further study details as provided by Saint Bernard Mission University:

Primary Outcome Measures:
  • The Changes of Amounts of Pain Killer Consumed for Scheduled Term Before and After PRP treatment. [ Time Frame: 1 month ] [ Designated as safety issue: No ]

Estimated Enrollment: 25
Study Start Date: December 2012
Estimated Study Completion Date: December 2014
Estimated Primary Completion Date: December 2013 (Final data collection date for primary outcome measure)

Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Sampling Method:   Probability Sample
Study Population

Athlete community


Inclusion Criteria:

  • Injury by professional sports and non professional sports

Exclusion Criteria:

  • Other basic disease holder
  Contacts and Locations
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No Contacts or Locations Provided
  More Information

No publications provided

Responsible Party: Saint Bernard Mission University Identifier: NCT01749839     History of Changes
Other Study ID Numbers: NCRM-SBMU0317
Study First Received: December 11, 2012
Last Updated: December 12, 2012
Health Authority: Switzerland: Federal Office of Public Health
Austlaria:National Health and Medical Research Council processed this record on October 19, 2014