Clinical Trials Logo

Wrist Fractures clinical trials

View clinical trials related to Wrist Fractures.

Filter by:

NCT ID: NCT01921062 Terminated - Clinical trials for Distal Radius Fracture

Motor Imagery in Rehabilitation After a Distal Radius Fracture

MIDRF
Start date: July 2011
Phase: N/A
Study type: Interventional

The aim of this study is to determine whether motor imagery training during the immobilisation period in patients with a distal radius fracture, results in an improved functional outcome compared to patients who do not perform motor imagery.

NCT ID: NCT01693094 Suspended - Clinical trials for Carpal Tunnel Syndrome

A Randomized Trial Measuring the Effect of Decision Aids on Patients' Satisfaction, Conflict of Decision-making and Clinical Outcome

Start date: June 10, 2014
Phase: N/A
Study type: Interventional

The investigators plan a prospective randomized controlled study that compares the treatment decisions made by patients who receive decision aids, as compared to patients treated with usual care and the American Society for Surgery of the Hand brochures. The investigators expect to enroll 126 patients.

NCT ID: NCT00988572 Completed - Dizziness Clinical Trials

Vestibular Rehabilitation for Patients With Fall-related Wrist Fractures

Start date: March 2009
Phase: N/A
Study type: Interventional

Dizziness has been identified as a risk factor for fall and vestibular asymmetry has been found among patients with fall-related wrist fractures as well as among patients with hip-fracture. Since wrist fracture is a risk factor for hip-fracture, much effort is focused on preventing falls for risk-groups. Therefore, it would be interesting to find out if it is possible to influence vestibular asymmetry with vestibular rehabilitation. The aim of this study is therefore to find out if vestibular rehabilitation can have any effect on vestibular function among patients with fall-related wrist fracture.

NCT ID: NCT00828685 Completed - Wrist Fractures Clinical Trials

Early Functional Outcomes After Closed Reduction With Pinning Versus Open Reduction Internal Fixation of Wrist Fractures

Start date: n/a
Phase: N/A
Study type: Interventional

The purpose of this study is to compare early return to function in patients treated with closed reduction percutaneous pinning and open reduction internal fixation in displaced fractures of the distal radius. Hypothesis: Wrist range of motion, grip strength and outcome at 2-3 months after injury are better in patients treated with open reduction, internal fixation (ORIF) than in patients treated with closed reduction percutaneous pinning techniques (CRPP). In addition patients treated with ORIF return to work at faster rates.

NCT ID: NCT00285961 Completed - Wounds and Injuries Clinical Trials

Evaluation of Cork Splint Materials Instead of Plaster Splint for Children

Start date: n/a
Phase: N/A
Study type: Interventional

This is an evaluation of the functionality and added value of cork splint materials instead of a plaster splint for children (3-11 years old).

NCT ID: NCT00175214 Completed - Osteoporosis Clinical Trials

Controlled Trial to Increase Detection and Treatment of Osteoporosis in Older Patients With a Wrist Fracture

Start date: January 2001
Phase: N/A
Study type: Interventional

The primary objective of this proposed research is to improve the quality of care for patients who present to the Emergency Department with osteoporosis and a fracture of the wrist, by increasing the use of proven efficacious osteoporosis treatment. This is the primary study outcome, and it is defined as starting any one of hormone therapy, a bisphosphonate, raloxifene, or calcitonin within 6 months of a fracture of the wrist. The study hypothesis is that a quality improvement intervention (with multiple components that include a notification system for primary care physicians, patient-specific reminders, locally generated treatment guidelines endorsed by opinion leaders, and patient education and counseling) will lead to increased use of proven efficacious osteoporosis treatments in patients eligible for secondary prevention. This hypothesis will be tested by comparing the intervention with usual care controls, in a prospective nonrandomized controlled trial.