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:

  1. Dislocated or history of dislocation.
  2. Patellar instability.
  3. Bony abnormality (trochlear groove hypoplasia or flat).
  4. Osteoarthritis of the knee 3rd and 4th grades.
  5. Infected knee.
  6. Varus and valgus knee.
  7. Rotational deformity of the lower extremity.
  8. Miserable malalignment triad.
  9. Anterior cruciate ligament, posterior cruciate ligament and medial collateral ligament rupture.
  10. History of fracture around knee.
  11. Focal Osteoarthritis of the lateral facet joint.
  12. 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.

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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