ClinicalTrials.gov
ClinicalTrials.gov Menu

Posterior Cruciate Ligament Reconstruction Using Knot/Press-fit Technique

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
ClinicalTrials.gov Identifier: NCT01200095
Recruitment Status : Completed
First Posted : September 13, 2010
Last Update Posted : September 13, 2010
Sponsor:
Information provided by:
Taipei Medical University WanFang Hospital

Brief Summary:
This study presents an arthroscopic-assisted PCL reconstruction using femoral knot/press-fit technique with a periosteum-enveloping graft in tibial tunnel. The investigators evaluated the results of patients with PCL ruptures, who undergoing PCL reconstruction using this unique technique.

Condition or disease
PCL TEAR

Study Type : Observational
Actual Enrollment : 30 participants
Observational Model: Case-Only
Time Perspective: Retrospective
Official Title: Non-hardware Posterior Cruciate Ligament Reconstruction Using Knot/Press-fit Technique With Periosteum-Evenloping Hamstrings Tendon Autograft
Study Start Date : January 2003
Actual Study Completion Date : December 2008

Resource links provided by the National Library of Medicine

U.S. FDA Resources





Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Ages Eligible for Study:   15 Years to 60 Years   (Child, Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
Patients with PCL tear who received surgery
Criteria

Inclusion Criteria:

  • PCL TEAR

Exclusion Criteria:

  • PL INSTBILITY

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01200095


Sponsors and Collaborators
Taipei Medical University WanFang Hospital
Investigators
Principal Investigator: Tai-Yuan Chuang Taipei Medical University WanFang Hospital

Responsible Party: Tai-Yuan Chuang, Department of Traumatology
ClinicalTrials.gov Identifier: NCT01200095     History of Changes
Other Study ID Numbers: 99045
First Posted: September 13, 2010    Key Record Dates
Last Update Posted: September 13, 2010
Last Verified: September 2010