Health Condition 1: O- Medical and Surgical
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Male and female patients aged >=18 years of age at the time of surgery who has undergone ACL reconstruction surgery with Adjustable Loop Button and PLDLA-βTCP interference screw during the index period of September 2018 to March 2022. 2. Patients who are willing to permit the research team to access their medical records and collect data for this study. 3. Patients who are willing to provide consent for participating in the study either by making a physical visit to the clinic (If their follow-up visit is scheduled or pending) or by answering the questionnaire telephonically.
Exclusion criteria
Exclusion criteria: 1. Patients who had suffered from any associated fractures, multi-ligament injuries or any other reconstructive surgeries apart from ACL during the index surgery. 2. Patients who have developed fractures/injury to the operated limb after the surgery.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1. To assess the postoperative functional outcomes after ACL reconstruction using arthroscopic implants (adjustable loop button and PLDLA-βTCP interference screw)Timepoint: One followup after EC approval (6 months to 3.5 years after surgery) | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. To assess the activity level in patients before and after ACL reconstruction surgery 2. To evaluate the knee-specific symptoms after ACL reconstruction surgery 3. To evaluate any adverse events after ACL reconstruction surgery Timepoint: One followup after EC approval (6 months to 3.5 years after surgery) | — |
Countries
India
Contacts
Sanjay Gandhi Postgraduate Institute of Medical Sciences