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Dislocations clinical trials

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NCT ID: NCT02185001 Terminated - Clinical trials for Torn Medial Patellofemoral Ligament

Repair of Medial Patellofemoral Ligament Compared to Conservative Treatment for First Time Patella Dislocation

Start date: October 2014
Phase: N/A
Study type: Interventional

Background: The forces involved in a patella dislocation event can cause significant collateral damage involving the articular cartilage of the patella femoral joint. As a result, prevention of recurrent patella dislocation and the associated disability and morbidity has generated significant interest in the orthopedic community. Historically, nonoperative treatment for first time patella dislocation has been problematic due to high redislocation rates. Nonoperative protocols generally involve bracing and/or immobilization, followed by physical therapy (1). Surgical approaches to recurrent patella dislocation, both soft tissue and boney realignment operations, have also had mixed results, including low success rates, associated complications, and variable rates of return to functional activity (2,3,4). This study is intended to compare the outcomes of a relatively low-risk Medial Patellofemoral Ligament (MPFL) direct repair procedure to conservative treatment. Methods/Design: This study is designed as a two arm randomized prospective trial. Approximately fifty subjects will be randomly assigned to either a surgical or non-operative arm by means of a computer randomized allocation program. All subjects will have X-Ray Images and Magnetic Resonance Imaging (MRI) to determine the site of the MPFL damage, and to determine if any excluding conditions exist. Subjects randomized to the surgical group will have repair of the MPFL. Routine aftercare will consist of physical therapy in a clinic that has agreed to follow our protocol. Subjects randomized to the nonoperative group will receive 2 weeks of patellar immobilization, followed by patellar stabilization bracing with physical therapy for approximately 12 weeks. Physical therapy will progress through five phases with the goal of gait normalization, full range of motion and return to sport. Both arms will be given outcome questionnaires and physical activity assessments before treatment, and at one, three, six, twelve, and twenty four month intervals. Discussion: This prospective randomized trial will investigate the results of direct repair of the medial patellofemoral ligament and conservative treatment by applying subjective outcome measures (Kujala scores), and exam findings to determine MPFL functional restoration or redislocation. Subjects will be examined in the clinic setting at 10 days, one month, and six months post trauma. Any reported recurrent dislocation or subluxation event will be documented during recovery. All subjects will receive merchant x-ray views at 3 months with manual lateral translation of the patella.

NCT ID: NCT00816647 Terminated - Clinical trials for Patellofemoral Osteoarthritis

A Prospective Randomized Study of Medial Patellofemoral Ligament (MPFL) Reconstruction

Start date: December 2008
Phase: N/A
Study type: Interventional

The operative management of chronic patellar instability has been controversial. Medial patellofemoral ligament reconstruction has gained success recently and might be superior to other soft-tissue procedures. The objective of this prospective study was to compare the clinical outcome after medial patellofemoral ligament reconstruction compared with medial reefing for chronic patellar instability.

NCT ID: NCT00580866 Terminated - Elbow Fracture Clinical Trials

Progressive Splinting Status Post Elbow Fractures and Dislocations

JAS
Start date: September 2006
Phase: N/A
Study type: Interventional

The purpose of this study is to help determine if a static stretching brace in addition to physical therapy decreases the incidence of secondary operations, increases range of motion, and individual patient function.

NCT ID: NCT00356837 Terminated - Fractures Clinical Trials

Diagnosing Extremity Fractures and/or Dislocations Using Ultrasound Presenting to the Emergency Department

Start date: August 2006
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the efficacy of ultrasound in diagnosing the presence or absence of extremity fractures or dislocations. Hypothesis: Can ultrasound be used as an accurate and effective method for determining the presence or absence of extremity fractures or dislocations? Is there a difference in amount of pain experienced prior to and after the ultrasound?

NCT ID: NCT00326352 Terminated - Clinical trials for Shoulder Dislocation

Comparison of Sedation/Analgesia: Midazolam/Morphine Vs Propofol/Remifentanil

Start date: July 2003
Phase: N/A
Study type: Interventional

For reduction of dislocated shoulder, sedation with propofol and remifentanil should give satisfactory operating conditions and pain relief, and significantly reduce the time to full recovery, compared with morphine and midazolam