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Fractures, Bone clinical trials

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NCT ID: NCT00408291 Completed - Fracture Clinical Trials

Evaluation of Treatment of Fractures of the Humerus With a Plate.

Start date: December 2011
Phase:
Study type: Observational

The purpose of this study is to study with the use of clinical and radiological parameters the treatment of three-part and four-part fractures with the Winsta PH osteosynthesis device (Fischer Medical).

NCT ID: NCT00398268 Recruiting - Child Clinical Trials

Dislocated Unstable Distal Both-Bone Forearm Fractures in Children

Start date: January 2006
Phase: N/A
Study type: Interventional

We create a follow-up study of Kirschner wire fixation of a unstable dislocated distal both-bone forearm fracture.

NCT ID: NCT00398242 Recruiting - Child Clinical Trials

Treatment of Stable Both-Bone Midshaft Forearm Fractures in Children

Start date: January 2006
Phase: N/A
Study type: Interventional

We create a randomized clinical trial between the treatment with above elbow armcast alone and the treatment of above elbow in combination with a short arm cast for stable midshaft both-bone forearm fractures.

NCT ID: NCT00397995 Recruiting - Child Clinical Trials

Undislocated Distal Both-Bone Forearm Fractures in Children

Start date: January 2006
Phase: N/A
Study type: Interventional

We create a randomized clinical trial between above- and below elbow cast to find out what kind of treatment is optimal for undislocated both-bone distal forearm fractures.

NCT ID: NCT00397852 Recruiting - Child Clinical Trials

Dislocated Stable Distal Both-Bone Forearm Fractures in Children

Start date: January 2006
Phase: N/A
Study type: Interventional

We create a randomized clinical trial between treatment with and without Kirschner wire fixation of a stable dislocated distal both-bone forearm fracture.

NCT ID: NCT00390741 Completed - Hip Fracture Clinical Trials

BHS4 - Bone/Muscle Changes Following Hip Fracture in Older White Women

Hip4
Start date: October 1998
Phase: N/A
Study type: Interventional

The major goals of this study are: 1. To conduct an intervention development study to evaluate the feasibility of implementing an exercise intervention for reduction losses in bone mineral density, muscle mass, and strength, and clinically relevant aspects of functioning following a hip fracture, and to obtain preliminary tests of the effective ness of these interventions. 2. To evaluate the effect of home-based exercise intervention on bone metabolism. 3. To evaluate the effects of hip fracture on bone metabolism. 4. To evaluate the effects of exercise and hip fracture on hormonal regulators. 5. To evaluate the association between markers of bone metabolism hormone regulators, and BMD. 6. To separate out the effects of hip fracture on bone turnover from those of aging in persons with low bone mineral density.

NCT ID: NCT00389844 Completed - Hip Fracture Clinical Trials

BHS5 - Testing the Effectiveness of the Exercise Plus Program

Hip5
Start date: July 2000
Phase: N/A
Study type: Interventional

The major goals of this study are: To implement a self-efficacy based intervention to strengthen efficacy beliefs related to exercise, decrease perceived barriers to exercise, and increase exercise behavior and overall activity of older women who have sustained a hip fracture. To test the effectiveness of the Exercise Trainer component of the intervention on exercise behavior, activity, efficacy expectations, barriers to exercise, performance behaviors, overall health status, mood, pain, fear of falling, falls and fall-related injuries at 2, 6, and 12 months following fracture.

NCT ID: NCT00387686 Terminated - Fractures Clinical Trials

A Phase 2/3 Multicenter, Controlled Trial Of rhBMP-2/CPM In Tibial Fractures

Start date: November 2006
Phase: Phase 2/Phase 3
Study type: Interventional

The primary objective of this study is to assess whether a single dose of rhBMP-2/CPM administered at the fracture site via percutaneous injection, in combination with standard of care, accelerates fracture union and return to normal function in subjects who have a closed diaphyseal tibial fracture when compared to standard of care alone.

NCT ID: NCT00384852 Completed - Fractures Clinical Trials

A Study of rhBMP-2/CPM in Closed Fractures of the Humerus

Start date: January 2007
Phase: Phase 2
Study type: Interventional

The primary objective of this study is to assess whether fracture union is accelerated in subjects with humeral fractures (proximal,diaphyseal) treated with conservative therapy (standard of care) and a single dose of rhBMP-2/CPM compared to subjects who receive standard of care alone.

NCT ID: NCT00384358 Completed - Fractures Clinical Trials

Feasibility And Safety Study Of rhBMP-2/CPM For Hip Fractures

Start date: December 2006
Phase: Phase 2
Study type: Interventional

The primary objective of this study is to assess the safety of administering rhBMP-2/CPM as an adjuvant to internal fixation in subjects with fractures of the proximal femur.