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Dislocations clinical trials

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NCT ID: NCT03070743 Recruiting - Clinical trials for Basilar Invagination Associated With Atlantoaxial Dislocation

Posterior Compression Distraction Reduction Technique System in the Treatment of BI-AAD

PCDR-BIAAD
Start date: July 2015
Phase: N/A
Study type: Observational

Posterior compression distraction reduction technique (PCDR) in the treatment of Basilar invagination associated with atlantoaxial dislocation

NCT ID: NCT03060655 Recruiting - Clinical trials for Fracture Dislocation

Study of PLGA-Mg Material in Clinical Orthopedics

Start date: August 2016
Phase: Phase 2
Study type: Interventional

The different proportion samples of PLGA-Mg were made in this study. Then, they would be placed in the femoral condyle of the New Zealand rabbits. The appropriate proportion of PLGA-Mg is obtained after the experiment, which will be used to make the plate or screw to fix the fragments. Then, the clinical role for bone will be assessed.

NCT ID: NCT02469818 Recruiting - Clinical trials for Shoulder Dislocation

Diagnostic Accuracy of Bedside Ultrasonography in the Management of the Shoulder Dislocations

Start date: January 2015
Phase: N/A
Study type: Observational

Shoulder dislocation is a common clinical presentation in the emergency department, comprising about 50 percent of all major joint dislocations. In the standart management of shoulder dislocations physicians generally need to see pre and post reduction x ray graphics. Ultrasonography is harmless way of evaluating shoulder and may be used in the management of the shoulder dislocations instead of the x ray evaluations.

NCT ID: NCT02463630 Recruiting - Clinical trials for Basilar Invagination Associated With Atlantoaxial Dislocation

Posterior Compression Distraction Reduction (CDR)Technique in the Treatment of BI-AAD

CDR
Start date: July 2014
Phase: Phase 3
Study type: Interventional

Posterior compression - distraction reduction technique (CDR) in the treatment of Basilar invagination associated with atlantoaxial dislocation

NCT ID: NCT02200744 Recruiting - Clinical trials for Joint Dislocation Reduction

Incidence of Recall After Procedural Sedation With Propofol in the Emergency Department

MEMOPROPO
Start date: April 2014
Phase: N/A
Study type: Observational

The purpose of this study is to determine the incidence of recall in patients managed in emergency department with a procedural sedation protocol using propofol in a population of 250 .

NCT ID: NCT02095093 Recruiting - Hip Osteoarthritis Clinical Trials

An Intelligent Instrument for Improved Leg Length and Hip Offset Accuracy in Total Hip Arthroplasty

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

Leg length discrepancies following total hip arthroplasty have been associated with nerve palsies, gait abnormalities, and lower back pain. Leg length discrepancies are related to poorer functional outcomes and patient dissatisfaction. Failure to restore femoral offset following total hip arthroplasty has been linked to decreased range of motion and abductor muscle strength, impingement, limping, higher dislocation rates, increased polyethylene wear, and loosening of implants. Computer navigation has shown to improve the accuracy of leg length and hip offset during total hip arthroplasty. The investigators research objective is to prove the accuracy of the Intellijoint HIP™ system for determining leg length and hip offset. The investigators hypothesis was that Intellijoint HIP™, an imageless intraoperative intelligent instrument, could improve the accuracy of leg length and hip offset during primary total hip arthroplasty. The investigators plan to study this hypothesis in humans by comparing the leg length and hip offset discrepancies produced with Intellijoint HIP™ to the standard at the investigators institution, which is a pin and outrigger system.

NCT ID: NCT02075775 Recruiting - Dislocations Clinical Trials

MOON Shoulder Instability-Cohort of Patients Undergoing Operative Treatment.

MOONSI
Start date: August 2012
Phase:
Study type: Observational [Patient Registry]

This project will be a multi-center, prospective longitudinal cohort for all patients undergoing primary shoulder instability surgery, excluding isolated SLAP repairs. We will be looking for risk factors for recurrent instability, revision surgery, and poor outcomes. Patients will be asked to complete the RAND-36, ASES, Shoulder Activity, EQ-5D and WOSI outcome measures, as well as demographic and socioeconomic information. Surgeons will complete a form after surgery with information on radiographic findings, physical exam, surgical findings, and the repair. Patients will wear a sling post-operatively, and follow standardized rehabilitation protocols, including physical therapy. Patients will be sent outcome questionnaires at 2, 6, 10, and 20 years after surgery.

NCT ID: NCT01206127 Recruiting - Clinical trials for Fuchs' Endothelial Dystrophy

DSAEK- Postoperative Positioning and Transplant Dislocation

Start date: September 2010
Phase: N/A
Study type: Interventional

Corneal transplant is a surgical procedure where a damaged or diseased cornea is replaced by donated corneal tissue (the graft) in its entirety (penetrating keratoplasty) or in part (lamellar keratoplasty). One type of lamellar keratoplasty is DSAEK (Descemet's Stripping Automated Endothelial Keratoplasty), where only the damaged posterior section of the cornea is replaced. The purpose of this study is to investigate how immediate postoperative positioning of the patient affects the dislocation rate of the corneal graft. Since this is a new surgical method, little scientific documentation has been published in this area.

NCT ID: NCT01111500 Recruiting - Clinical trials for Glenohumeral Joint Dislocation

Immobilization After an Anterior Glenohumeral Joint Dislocation With a Bankart Lesion

Start date: July 2007
Phase: N/A
Study type: Interventional

Glenohumeral joint dislocation is the most frequent joint dislocation with a prevalence of 1.7/100000 citizens/year. It is treated by reduction, under sedation or anaesthesia, followed by an immobilization of the arm. The purpose of the study is to evaluate the healing of the labrum in first time anterior glenohumeral joint dislocation with a Bankart lesion in young patients by comparing an external rotation brace to an internal rotation brace to immobilize the injured arm.

NCT ID: NCT01110304 Recruiting - Clinical trials for Acromio-clavicular Joint Dislocation (Type III)

Acromio-clavicular Dislocation Type III - Conservative Treatment Versus Surgical Hook Plate Treatment

Start date: May 2007
Phase: N/A
Study type: Interventional

Acromio-clavicular (AC) joint dislocation corresponds to 8.6% of all joint dislocations and represents a major injury to the shoulder girdle. The nature of the treatment is decided according to the severity of the lesion. The purpose of this study is to determine whether the surgical treatment is required or not for type III AC joint dislocations.