Clinical Trials Logo

Dislocations clinical trials

View clinical trials related to Dislocations.

Filter by:

NCT ID: NCT01544725 Completed - Fracture Clinical Trials

Ketamine-propofol Versus Ketamine Alone for Procedural Sedation in Adults

Start date: April 2012
Phase: Phase 4
Study type: Interventional

Using Ketamine for procedural sedation in adults is often uncomfortable for emergency physicians because of the significant proportion of patients experimenting recovery agitation. The investigators believe that combining propofol to ketamine, the proportion of recovery agitation will be significantly lowered. The objectives of this double-blinded, randomized controlled trial are to compare the proportion of recovery agitation in adults receiving procedural sedation with ketamine-propofol versus ketamine alone, and to compare the proportion of other classical procedural sedation side-effects and parameters such as respiratory depression, hypotension, sedation duration, time of recovery, procedural failures, and levels of satisfaction.

NCT ID: NCT01528319 Completed - Clinical trials for Shoulder Dislocation

Open-Label Study for Shoulder Dislocation Using MG-1

MG-1
Start date: December 2011
Phase: N/A
Study type: Interventional

To evaluate the efficacy and safety of arthroscopic Bankart repair using MG-1 for dislocation of shoulder

NCT ID: NCT01479738 Completed - Clinical trials for Recurrent Dislocation of Hand

Proximal Interphalangeal Joint Arthroplasty Using a Graft From the Capitate

PIPPC
Start date: January 2005
Phase: N/A
Study type: Interventional

The capitate had a widened distal base. The distal articulation can be used for proximal interphalangeal (PIP) articula reconstruction.

NCT ID: NCT01402778 Completed - Infection Clinical Trials

Fixation of Thoracic Epidurals Influencing Catheter-related Infections and Dislocation

TDPAFD
Start date: January 2011
Phase: N/A
Study type: Observational

Major interest in our investigation is to find out whether distinct fixation techniques influence catheter dislocation and/ or incidence of local inflammation. A systematic comparison of two different fixation techniques with regard to catheter location, analgetic potential and signs of local inflammation will be conducted. To ensure identical patients groups allocation will be strictly randomized. Furthermore, both patient groups will receive identical pain medication via the peridural catheter in situ. All catheter tips will be screened microbiologically after removal.

NCT ID: NCT01375218 Completed - Clinical trials for Hip Dislocation, Congenital

Efficacy and Satisfaction Comparing Two Braces in the Treatment of Developmental Dysplasia of the Hip (DDH) in Infants

Start date: June 2011
Phase: Phase 4
Study type: Interventional

The purpose of this study is to 1) evaluate the effectiveness of the Plastizote abduction brace compared to the Pavlik harness in the treatment of developmental dysplasia of the hip (DDH) and 2) compare parent/caregiver satisfaction between the Plastizote abduction brace and the Pavlik harness. The investigators hope to learn which brace treatment is best for a definable population so the appropriate brace can be chosen initially avoiding the time, expense, and frustration of a failed technique.

NCT ID: NCT01353352 Completed - Clinical trials for Fracture of Cervical Spine

Evaluation of the Nursing C-Spine (Phase IV)

Start date: January 2008
Phase: Phase 4
Study type: Interventional

Neck injuries are a common problem among blunt trauma victims with more than 8,000,000 cases being seen annually in U.S. and Canadian EDs. While the majority of these cases represent soft tissue injuries, 30,000 patients suffer cervical spine fractures or dislocations and approximately 10,000 suffer spinal cord injury. There are no readily available national Canadian data on ED visits such as those provided by the U.S. National Hospital Ambulatory Medical Care Survey. The prevalence of potential neck injury can, however, be reasonably estimated for Canadian EDs. Extrapolation, on a population basis, from reliable U.S. figures suggests that 1.3 million potential neck injury patients are seen annually in Canada. Only 0.9% of these patients are found to have cervical spine fractures or dislocations.

NCT ID: NCT01274884 Completed - Clinical trials for Acromioclavicular Joint Dislocation

Tightrope Fixation of Acromioclavicular Joint Dislocation - a Prospective Series

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

Several surgical techniques are used for the treatment of acute acromioclavicular joint dislocations. The investigators investigate a new method using arthroscopic repair using the Tightrope fixation device.

NCT ID: NCT01205763 Completed - Clinical trials for AC Joint Dislocation

Evaluation of Effects of Clavicular Hook Plate on Subacromial Space

Start date: December 2007
Phase: N/A
Study type: Observational

In this study, the investigators intend to demonstrate that the hook plate may have adverse effects on subacromial structures even with a short period of hardware retention. The investigators also sought to determine if musculoskeletal sonography could be used as a tool to demonstrate shoulder pathology such as subacromial impingement or rotator cuff tear in patients receiving hook plate fixation. The clinical results of patients receiving hook plate fixation, specifically bony union, pain relief, shoulder function and range of motion (ROM), were also evaluated.

NCT ID: NCT01086202 Completed - Rotator Cuff Tear Clinical Trials

Clinical Outcome Comparison Between Medial and Lateral Offset Reverse Shoulder Arthroplasty

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

The purpose of this study is to prospectively evaluate two FDA approved implant designs for the Tornier Reverse Shoulder arthroplasty. The small difference in design is the amount of offset each implant has. This offset may improve clinical outcomes in the patient population. There have been no clinical comparative studies between these two designs in the literature to date. We would like to follow these patients for two years after implantation of the reverse shoulder and evaluate their radiographs, pain scores, and shoulder functional scores. this would be the first randomized prospective single blinded study of its kind.

NCT ID: NCT01059721 Completed - Patella Dislocation Clinical Trials

Outcome After Soft Tissue Realignment of the Tibial Insertion of the Patella Tendon

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

Soft tissue realignment of the tibial insertion of the patella tendon is a simple operative technique for treating dislocation of the patella in childhood and adolescence. It is performed in children with either recurrent dislocation or complicated primary dislocation in cases with malalignment or maltracking of the patella and a lateralised tibial tuberosity. It can be performed in patients with open epiphyses. We investigate long-term outcome after this procedure.