Health Condition 1: M236- Other spontaneous disruption of ligament(s) of knee
Conditions
Interventions
None listed
Sponsors
Silver Research and Ethics Committee
Eligibility
Inclusion criteria
Inclusion criteria: All patients who underwent ACL reconstruction using hamstring graft suspensory fixation on both the femoral and tibial ends utilizing the Internal Brace Augment will be included in the study
Exclusion criteria
Exclusion criteria: All other forms of ACL reconstruction
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Percentage of graft integration at the femoral end. Percentage of graft integration at the tibial end. Timepoint: Percentage of graft integration at the femoral end at 6 months Percentage of graft integration at the tibial end at 6 months | — |
Secondary
| Measure | Time frame |
|---|---|
| To assess the clinical outcome of patients having undergone ACL reconstruction using Hamstring graft augmented with INternal Brace system. To compare integration percentages and clinical outcomesTimepoint: 6 months | — |
Countries
Bangladesh, India
Contacts
Public ContactRoncy Savio Kuruvilla
Christian Medical College Hospital
Outcome results
None listed