NCT Number: NCT00221273
Use of Graft Tensioner Device in ACL (Knee) Repair
Compares tension of an ACL graft when using a commercial device vs. the tension of the graft applied by a physician during surgery.
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Notify MeKey information
Conditions
Age range
19 year and older
Sex eligibility
All sexes
Study type
Interventional
Phase
Not applicable
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Torn ACL amenable to surgery
Exclusion criteria
Treatment and study plan
Primary outcomes
-
Endpoints Measured at 6, 12, 18 months post op compared to pre-op
Sponsors and collaborators
Lead sponsor
University of British Columbia
Other
Registry information
Official study title
Randomized Clinical Trial to Assess the Clinical Effectiveness of a Measured Objective Tensioning in Hamstring ACL Reconstruction
Important dates
- Study start
- 2010
- Primary completion
- 2012
- Study completion
- 2012
- First posted
- Sep 22, 2005
- Registry last updated
- Mar 3, 2017
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.