Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
The main purpose of this study is to determine if there is a difference in graft re-injury/failure rates between participants that have had an ACL reconstruction with a STG, BPTB or QT autograft. Additionally, to compare quality of life, patient reported outcomes and functional performance after ACL reconstruction with STG, BPTB and QT.
The main purpose of this study is to determine if there is a difference in graft re-injury/failure rates between participants that have had an ACL reconstruction with a STG, BPTB or QT autograft. Additionally, to compare quality of life, patient reported outcomes and functional performance after ACL reconstruction with STG, BPTB and QT.
Quasi-randomized clinical trial
Not provided
Not provided
Not provided
Not provided
| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Quads tendon | Active Comparator | The graft tissue will be quadriceps tendon |
|
| Hamstring | Active Comparator | Semitendinosus and gracilis will be used for graft |
|
| BPTB | Active Comparator | Bone patellar tendon bone graft to be used. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| ACL reconstruction - graft choice | Procedure | Use of 3 different ipsilateral autograft options |
|
| Measure | Description | Time Frame |
|---|---|---|
| graft re-injury (re-rupture, partial tear) or graft failure | ) Diagnosis of a complete graft re-rupture requires all of the following criteria to be met:
| 24 months |
| Measure | Description | Time Frame |
|---|---|---|
| SANE | 24 months | |
| Knee laxity | KT1000 Knee Laxity Arthrometer | 24 months |
| Concentric maximal strength |
Not provided
Inclusion Criteria:
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Pan Am Clinic | Winnipeg | Manitoba | R3M3E4 | Canada |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| ID | Term |
|---|---|
| D000070598 | Anterior Cruciate Ligament Injuries |
| ID | Term |
|---|---|
| D007718 | Knee Injuries |
| D007869 | Leg Injuries |
| D014947 | Wounds and Injuries |
Not provided
Not provided
Prospective quasi-randomized clinical trial
Not provided
Not provided
The clinical assessments will be done by someone blinded to the arm of the study the patient is in.
Knee flexion and extension strength - biodex |
| 24 months |
| Pain log | type and quantity of pain medication use | 3 weeks post operative |
| ACL-QOL | 24 months |
| SF-12 | 24 months |