Clinical Trials Logo

Dislocations clinical trials

View clinical trials related to Dislocations.

Filter by:

NCT ID: NCT02228226 Completed - Clinical trials for Shoulder Dislocation

Follow-up Study After Bankart Repair Using MG-1

Start date: August 2014
Phase: N/A
Study type: Observational

Long term follow-up of patients those who underwent arthroscopic Bankart repair using MG-1 for dislocation of shoulder to evaluate anchor bone hole condition and ossification.

NCT ID: NCT02192476 Completed - Clinical trials for Subluxation of Inferior Shoulder

Efficacy of CTPT Method in the Treatment of Post Stroke Shoulder Subluxation

CTPT
Start date: June 2013
Phase: Phase 1
Study type: Interventional

california tri-pull taping (CTPT) method might be effective in reducing shoulder subluxation, pain, and improving active flexion range (AFLXN) range of motion, and functional recovery after stroke.

NCT ID: NCT02182752 Completed - Clinical trials for Shoulder Dislocation

The Effect of Tramadol on Interscalene Brachial Plexus Block

Start date: April 2013
Phase: Phase 2
Study type: Interventional

The purpose of our study is to evaluate the effect of tramadol as an adjunct to ropivacaine local anesthetic solution in interscalene brachial plexus block for shoulder surgery.

NCT ID: NCT02131987 Completed - Clinical trials for Femoral Neck Fracture

Radiological Riskfactors for Dislocation of Hip Hemiarthroplasty

RRDHHR
Start date: January 2006
Phase: N/A
Study type: Observational

Between January 1 2006 and December 31 2013, at our department 324 patients underwent hemiarthroplasty (HA) for displaced femoral-neck fracture with a bipolar prosthesis (Variokopf, Link®, Germany) by the use of the posteriolateral approach. Patients with pathological fractures and HA performed with direct lateral approach were excluded. A retrospective cohort study were conducted. Patients with prosthetic dislocation formed one group and patients without dislocation formed the control group. As standard, post surgery radiographs (anteroposterior and lateral) were taken. After these were performed patient started weight bearing as soon as possible. Clinical data regarding patient demographics, details of the surgical procedure and the medical comorbidities were collected by the use of patient and operative records. Radiological analysis with position evaluation was performed using the post surgery radiographs by measuring Wiberg angle, inequality of leg length and femoral offset of the prostheses and compared with non-operated hip joint using the post surgery x-ray images. Our hypothesis were that patients with single- or recurrent dislocations had shortened postoperative leg length, decreased femoral offsed and a Wiberg angle less than 25 degrees.

NCT ID: NCT02062450 Completed - Femur Head Necrosis Clinical Trials

Observational Study Evaluating Outcomes of Hip Arthroplasty Using Tornier Dual Mobility Acetabular Cup

Start date: May 2013
Phase: N/A
Study type: Observational

The purpose of this study is to demonstrate the performance and reliability of Tornier "Dual Mobility Cup" used during primary total hip replacement or hip replacement revision surgery at least 24 months post-insertion.

NCT ID: NCT02062437 Completed - Hip Replacement Clinical Trials

Clinical and Radiological Results of Total Hip Arthroplasty Using a Ceramic Friction Pair

CERAM
Start date: September 2013
Phase: N/A
Study type: Observational

The aim of this study is to assess safety and general performance of total hip arthroplasty, composed of a Meije Duo® femoral stem associated with a Dynacup® cup, and using the friction pair Biolox® Delta Ceramic.

NCT ID: NCT01644227 Completed - Osteoarthritis Clinical Trials

Dual Mobility Cup in Total Hip Arthroplasty Preventing Dislocation in Patients at Risk

Start date: June 2012
Phase: N/A
Study type: Observational

Retrospectively study reviewing 34 patients operated with dual mobility cups in total hip arthroplasty between January 2009 and June 2012 at Sundsvall Hospital. Hypothesis: The dual mobility socket reduce the rate of dislocation in patient at high risk but increase the incidence of postoperative infection.

NCT ID: NCT01585467 Completed - Clinical trials for Shoulder Dislocation

Anterior Shoulder Dislocation

Start date: February 2010
Phase: N/A
Study type: Observational

To compare and validate the two clinical algorithms

NCT ID: NCT01583465 Completed - Clinical trials for Arthritis, Rheumatoid

Efficacy of Aquamantys for Reducing Transfusions With Anterior Supine Intermuscular Approach Total Hip Arthroplasty

Aquamantys
Start date: October 2009
Phase: N/A
Study type: Interventional

The purpose of this study is to establish whether or not there is a clinical advantage to the use of Aquamantys® System from Medtronic Advanced Energy (formerly Salient Surgical Technologies) in patients undergoing primary total hip arthroplasty via the anterior supine intermuscular surgical approach in terms of blood loss, transfusion and wound healing. Wound healing will be assessed by a blinded observer and based upon a simple and subjective criteria: a) as expected, b) better than expected or c) worse than expected. The blinded observer is experienced in the care of the surgical patient and wound evaluation.

NCT ID: NCT01549912 Completed - Clinical trials for Shoulder Dislocation

Results of Rotator Cuff Repair

Start date: February 2012
Phase: N/A
Study type: Observational

The primary objective of this research is to examine the result of rotator cuff repairs following acute shoulder dislocations and to investigate whether timing of surgery following acute shoulder dislocations affects patients perception of pain, function, and strength following surgery.