- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04313556
Clinical Outcome of Arthroscopic Lateral Release for Lateral Patellar Compression Syndrome
March 17, 2020 updated by: Sherwan Ahmed Ali Hamawandi, Hawler Medical University
We performed a prospective case series study of 48 patients who suffered Lateral patellar compression syndrome who were diagnosed by clinical examination and confirmed by M.R.I. and failed conservative management and underwent isolated arthroscopic lateral patellar retinaculum release in Erbil Teaching Hospital, PAR Private Hospital and Hawler Private Hospital between December 2016 and August 2019.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
48
Phase
- Not Applicable
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
19 years to 45 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Lateral patellar compression syndrome proved by clinical,MRI and Arthroscopic examination
Exclusion Criteria:
- Dislocated or history of dislocation.
- Patellar instability.
- Bony abnormality (trochlear groove hypoplasia or flat).
- Osteoarthritis of the knee 3rd and 4th grades.
- Infected knee.
- Varus and valgus knee.
- Rotational deformity of the lower extremity.
- Miserable malalignment triad.
- Anterior cruciate ligament, posterior cruciate ligament and medial collateral ligament rupture.
- History of fracture around knee.
- Focal Osteoarthritis of the lateral facet joint.
- Chondral lesion (Outerbridge 3 and 4).
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Other: Lateral patellar release
Arthroscopic lateral patellar retinacular release
|
Arthroscopic lateral patellar reticular release
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Lysholm Knee Score
Time Frame: 12 months
|
Eight sections are assessed to produce an overall score on a scale of 0 to 100.
Then an assignment is given as "excellent" for 95 to 100 points; "good" for 85 to 94 points, "fair" for 65 to 84 points, or "poor" for less than 65 points
|
12 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
December 4, 2016
Primary Completion (Actual)
August 1, 2019
Study Completion (Actual)
August 30, 2019
Study Registration Dates
First Submitted
March 16, 2020
First Submitted That Met QC Criteria
March 17, 2020
First Posted (Actual)
March 18, 2020
Study Record Updates
Last Update Posted (Actual)
March 18, 2020
Last Update Submitted That Met QC Criteria
March 17, 2020
Last Verified
March 1, 2020
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- HMU/Sherwan8
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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