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Fractures, Bone clinical trials

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NCT ID: NCT02058329 Terminated - Depression Clinical Trials

A Geriatric Home Visit Program to Reduce Post-Hip Fracture Complications

Start date: November 2008
Phase: N/A
Study type: Interventional

The overall goal of the project is to reduce the incidence of post hip fracture morbidity and mortality by conducting geriatric fellow periodic home visits.The assessment will be multidisciplinary and will include assessments of functional status, depression, environmental risks and medical conditions. This group will be compared against a group followed by the usual standard of care post hip fracture.

NCT ID: NCT02057601 Completed - Postoperative Pain Clinical Trials

Postoperative Analgesia for Fractured Neck of Femur With Periarticular Infiltration of Local Anaesthetic

Start date: January 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to determine that periarticular levobupivacaine infiltration after surgical fixation of fractured neck of femur will improve the early postoperative pain sensation.

NCT ID: NCT02056834 Completed - Clinical trials for Closed Proximal Tibial Fracture AO-OTA 42

chronOS Inject in Proximal Tibial Fractures

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

The primary objective of this study is to observe the safety, the radiological and clinical outcomes of chronOS Inject after having been used as bone void filler in internal fixation of proximal tibial fractures.

NCT ID: NCT02056288 Terminated - Clinical trials for Supracondylar Fractures

A Comparison of UGSB and GA to IV Narcotics and GA for Post-Op Pain in Children With Supracondylar Fractures.

Start date: March 10, 2011
Phase: Phase 4
Study type: Interventional

This study compares nerve blocks to IV pain medicines in children with broken arms. We are trying to see if blocking the nerves in the broken arm results in better pain control and less side effects than injections of morphine into a vein after surgery for a broken elbow.

NCT ID: NCT02052206 Completed - Clinical trials for Osteoarthritis of the Shoulder

Reconstruction of Complex Proximal Humeral Fractures.

Start date: March 2014
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the accuracy of shoulder replacement surgery in realization a computer assisted 3D planning compared to conventional 2D planning.

NCT ID: NCT02050698 Recruiting - Treatment Clinical Trials

Hard-soled Shoe Versus Short Leg Walking Cast for a Fifth Metatarsal Avulsion Fracture: A Randomized Multicenter Noninferiority Trial

Start date: January 2014
Phase: N/A
Study type: Interventional

Fifth metatarsal avulsion fractures are common and can usually be treated conservatively. Symptomatic care consisting of protected weightbearing in a hard-soled shoe, air-cast walking boot, or below-knee walking cast have been successful. Several papers reported that early rehabilitation may decrease ankle stiffness, muscle and bone atrophy, and aids in early return to activities. However, early motion of the ankle joint may have the risk of displacement of the fifth metatarsal avulsion fractures. However, studies using hard-sole shoe for protected weightbearing and allowing motion of the ankle joint had successful results. Clapper et al. compared the results of hard-soled shoe and walking cast for a fifth metatarsal avulsion fracture and reported that all avulsion fractures healed uneventfully and that the results were similar between the two. However, this was not a randomized controlled trial. Devices such as air-cast walking boot, plaster slipper, or Jone's dressing can also be used for the treatment. However, we decided to compare results of hard-soled shoe and short leg walking cast for the treatment of a fifth metatarsal avulsion fracture. We hypothesized that the 100mm visual analogue scale (VAS) assessed on 6 months after a fifth metatarsal avulsion fracture treated with protected weightbearing in a hard-soled shoe is not inferior to protected weightbearing in a short leg walking cast but is superior to short leg walking cast with respect to time to return to normal daily life and patient's satisfaction.

NCT ID: NCT02049931 Completed - Clinical trials for Compression Fracture

Comparison of Treatments of Osteoporotic Compression Fracture Using Rigid Brace, Soft Brace, and no Brace

Start date: December 2012
Phase: N/A
Study type: Interventional

The treatment outcomes in the treatment without brace would be non-inferior to those in use of rigid or soft brace.

NCT ID: NCT02047955 Active, not recruiting - Clinical trials for Shoulder Arthroplasty and Fracture Repair

Tornier Shoulder Outcomes Study to Examine Safety and Functional Outcomes in Shoulder Arthroplasty and Fracture Patients

Start date: March 2014
Phase:
Study type: Observational [Patient Registry]

The Tornier Shoulder Outcomes Study is designed to collect safety and efficacy data on designated commercially available Tornier Shoulder repair products. In addition, this study will provide performance data for use in education, marketing materials, peer-reviewed publications and support research and development of future products.

NCT ID: NCT02045537 Active, not recruiting - HIV Clinical Trials

Retrospective Study to Determine the Incidence of Bone Fractures in HIV-infected Patients in Spain

INFOHS
Start date: June 2013
Phase:
Study type: Observational

Study to determine the incidence of Bone Fractures in HIV infected patients in Spain

NCT ID: NCT02038686 Completed - Clinical trials for Unstable Proximal Femoral Fracture

Treatment of Unstable 31.A2 and 31.A3 Trochanteric Fractures. Randomised Comparison of the Proximal Femoral Nail PFN-A Short and the PFN-A Long.

PFN-A
Start date: January 2014
Phase: N/A
Study type: Interventional

1. Introduction: Controversy exists with regard to whether to treat AO/OTA (Orthopaedic Trauma Association) 32.A2 - 32-A3 fractures of the proximal part of the femur with an intramedullary short PFN-A or long PFN-A. A prospective, randomized, controlled trial is performed to compare the outcome treatment of these unstable fractures of the proximal part of the femur with either a short PFN-A (170-240mm) or long PFN-A (300-420mm). 2. Objectives and Hypothesis The hypothesis is that the Short PFN-A would have fewer complications than Long PFN-A Main Objective: Is defined as Total number of complications between PFN-A short and PFN-A long. Outcome measures were subdivided into preoperative, perioperative and post-operative. Follow up data at four weeks, three months and one year. Secondary objectives: Complete and uneventful radiological and clinical healing of the fracture. Revision operations (related to the failure of primary treatment) and mortality. Baseline characteristics were documented pre-operatively: Outcome measures were subdivided into intra-operative, post-operative and follow up data at four weeks, three months and one year. 3. Methodology: One hundred and eighty eight patients presenting with an AO/OTA 31-A2 and 31-A3 fracture of the proximal part of the femur will be randomized, at the time of the admission, to fixation with use either a short PFN-A or a long PFN-A.