Patellar Dislocation Clinical Trial
Official title:
Clinical Outcomes Following Patellar Dislocation in Young Athletes
NCT number | NCT03040232 |
Other study ID # | 2011-1984 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | January 2016 |
Est. completion date | June 2018 |
Verified date | July 2020 |
Source | Children's Hospital Medical Center, Cincinnati |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of this study is to identify predictors of future injury and disability following LPD. The investigators' long term goal is to improve longitudinal outcomes of athletes with LPD following surgical and non-surgical management. Currently, there is limited information available to clinicians regarding appropriate criteria for returning athletes to sports participation following LPD. The evidence produced by this study will provide necessary information to develop appropriate rehabilitation strategies that may reduce the risk for future patellar instability and associated patellofemoral joint dysfunction and pain.
Status | Completed |
Enrollment | 50 |
Est. completion date | June 2018 |
Est. primary completion date | December 2017 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 12 Years to 25 Years |
Eligibility |
Inclusion Criteria: - Participants with LPD who have been managed with non-surgical rehabilitation, pre-surgical rehabilitation, and medial patellofemoral ligament reconstruction (MPFL-R) may be included. - Participants may be included in this study is they have completed supervised rehabilitation and have been cleared to return to sports participation by their physician. Exclusion Criteria: 1. lower extremity orthopedic surgeries other than procedures for patellar instability 2. lower extremity injuries within the last 3 months other than patellar dislocation 3. neurological disorders 4. medical conditions that might affect neuromuscular performance. |
Country | Name | City | State |
---|---|---|---|
United States | Cincinnati Childrens Hospital Medical Center | Cincinnati | Ohio |
Lead Sponsor | Collaborator |
---|---|
Children's Hospital Medical Center, Cincinnati |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | change in biomechanical assessment using motion analysis | measure changes in biomechanics between groups using motion analysis with particular interest in knee valgus measures | 6 months |
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