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Fractures, Bone clinical trials

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NCT ID: NCT00250302 Completed - Tibial Fracture Clinical Trials

Autologous Implantation of Mesenchymal Stem Cells for the Treatment of Distal Tibial Fractures

Start date: April 2009
Phase: Phase 1/Phase 2
Study type: Interventional

Mesenchymal stem cells are found in bone marrow, and have the ability to differentiate into different tissue types. The primary objective of the study is to examine the safety of using such cells to treat patients suffering from distal tibial shaft fractures. The cells will be isolated from the patient's bone marrow, loaded onto a carrier and implanted locally at the fracture site.

NCT ID: NCT00239889 Completed - Forearm Fracture Clinical Trials

Efficacy and Safety of Salmon Calcitonin Nasal Spray in Improving Muscle Strength and Reducing Pain After Forearm Fracture in Postmenopausal Women

Start date: March 2002
Phase: Phase 4
Study type: Interventional

Calcitonin has been used for many years for treating osteoporosis in postmenopausal women, and it has been shown that calcitonin reduces pain after spine and hip fracture in women with osteoporosis. Therefore, this study assesses the safety and efficacy of salmon calcitonin nasal spray on muscle strength after a forearm fracture, pain, quality of life and fracture healing in postmenopausal women.

NCT ID: NCT00211237 Completed - Cancer Clinical Trials

CAFE Study - Cancer Patient Fracture Evaluation

CAFE
Start date: May 2005
Phase: N/A
Study type: Interventional

The primary objective of this study is to evaluate the safety and effectiveness of balloon kyphoplasty treatment for painful, acute, vertebral compression fractures (VCFs) as compared to standard non-surgical therapy in patients with cancer.

NCT ID: NCT00208442 Completed - Osteoarthritis Clinical Trials

A Randomised Single Centre Study to Compare the Long-term Wear Characteristics of Marathon™ and Enduron™ Polyethylene Cup Liners in Primary Total Hip Replacement

Start date: June 1, 2001
Phase: Phase 4
Study type: Interventional

The purpose of this study is to compare the performance and compare the wear characteristics of two polyethylene cup liners, Marathon™ and Enduron™, in the treatment of patients with hip joint disease requiring a total hip replacement. Patients who enter the study will be randomly allocated to one of the polyethylene cup liners, Marathon™ or Enduron™ and will be evaluated at regular intervals using clinical and x-ray assessments.

NCT ID: NCT00206011 Completed - Clinical trials for Condylar Neck Fractures

Open Versus Endoscopic Surgery of Craniomaxillofacial (CMF) Condylar Neck Fractures

Start date: April 2003
Phase: Phase 4
Study type: Interventional

This study is a comparison of open surgery versus an endoscopic approach in condylar neck fractures; it will look at functional outcome, cosmetic outcome and patient satisfaction.

NCT ID: NCT00205985 Completed - Scaphoid Fracture Clinical Trials

Operative Versus Conservative Treatment of Scaphoid Fractures

Start date: December 2003
Phase: Phase 4
Study type: Interventional

The aim of this study is to compare the time to return to previous activity level between operative treatment and non-operative cast immobilization of patients with an acute complete fracture of the middle part of the scaphoid, without any dislocation or comminution visible CT-scan.

NCT ID: NCT00205972 Completed - Clinical trials for Humerusshaft Fractures

Non Randomized Humerusshaft Fracture

Start date: December 2000
Phase: Phase 4
Study type: Interventional

The aim of the study is to radiologically compare the fracture healing as well as the functional treatment outcome of conservative and operative treatment of defined humerusshaft fractures after 6w./12w./and 12 month based on the modified "constant score".

NCT ID: NCT00205959 Completed - Clinical trials for Proximal Humeral Fracture

LPHP-Philos-PHN Conservative Treatment

Start date: August 2002
Phase: Phase 4
Study type: Interventional

The aim of the study is to compare the results regarding fracture healing and functional outcome after the treatment of proximal humeral fractures with the four different treatment methods after 12w./6months and 12 months based on radiological evaluation as well as the "constant score" and the "neer score".

NCT ID: NCT00197496 Completed - Hip Fracture Clinical Trials

Body Weight Supported Treadmill Training Following Hip Fracture

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

Achieving independent ambulation is an important goal of hip fracture rehabilitation, as it is predictive of returning to the community and of future health problems. Current research regarding post-hip fracture rehabilitation is sparse. Body weight supported treadmill training (BWSTT) is a novel approach to retrain walking abilities. BWSTT may be ideal for retraining walking after hip fracture, as it is task-specific and alleviates the demands of maintaining balance while walking skills are trained. The use of the harness may provide a sense of security for the patient, facilitating walking training. The proposed project will investigate the feasibility and tolerability of BWSTT after hip fracture, and its impact on function, mobility, quality of life and fear of falling. It is hypothesized that BWSTT 3-5 times weekly in acute hip fracture patients will improve function, mobility, quality of life and reduce fear of falling.

NCT ID: NCT00190944 Completed - Colles' Fracture Clinical Trials

Effects of Teriparatide on Distal Radius Fracture Healing

Start date: December 2004
Phase: Phase 2
Study type: Interventional

Effects of Teriparatide on Distal Radius Fracture Healing