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Spinal Fractures clinical trials

View clinical trials related to Spinal Fractures.

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NCT ID: NCT01123512 Completed - Spinal Fractures Clinical Trials

The Kiva® System as a Vertebral Augmentation Treatment

KAST
Start date: July 2010
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the safety and effectiveness of the Kiva VCF Treatment system in comparison to balloon kyphoplasty for the treatment of osteoporotic vertebral compression fractures of the thoracic or lumbar spine.

NCT ID: NCT01120197 Completed - Osteoporosis Clinical Trials

Study of Effect of Exercise With Osteoporosis and Vertebral Fracture

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

The aim of this randomized controlled trial is to evaluate the effectiveness for health-related quality of life (HRQOL) of a 3-month course of exercises for a group of postmenopausal women with osteoporosis who has at least one vertebral fracture versus a control group (undertaking their usual activities). The course of exercises is devised in accordance with methods recommended in "Rehabilitation treatment guidelines in postmenopausal and senile osteoporosis".

NCT ID: NCT00994032 Completed - Osteoporosis Clinical Trials

Quality of Life After Vertebroplasty Versus Conservative Treatment in Patients With Painful Osteoporotic Vertebral Fractures

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

The purpose of this study is to determine whether percutaneous vertebroplasty is able to improve long-term quality of life in patients with pain secondary to osteoporotic vertebral fractures, compared to conventional medical treatment.

NCT ID: NCT00749242 Completed - SPINAL Fracture Clinical Trials

Comparative Study of Balloon Kyphoplasty and Conservative Treatment

TRAUMAA1-2-3
Start date: December 2007
Phase: Phase 4
Study type: Interventional

This study will compare two treatments in acute stable traumatic vertebral fractures (types A1, A2 and A3.1 in MAGERL Classification). The two treatments are the followings: 1. Conservative Orthopedic Management consisting of brace and pain medication. 2. Percutaneous Balloon Kyphoplasty, a variant of Vertebroplasty, in which a balloon is first placed into the fractured vertebra and inflated with fluid in order to create a cavity. This may restore part of the vertebral height loss due to the fracture and facilitate the injection of the cement with low pressure. The primary outcome will be the variation in the angle of Regional Vertebral Kyphosis (or, in the case of asymmetrical fractures, the angle of lateral vertebral inclination) between inclusion and one year follow-up. It will indicate if Balloon Kyphoplasty is able to restore vertebral height of the fractured vertebra better than Conservative Orthopedic Management.

NCT ID: NCT00749086 Completed - Clinical trials for Osteoporotic Vertebral Fracture

Comparison of Balloon Kyphoplasty and Vertebroplasty in Subacute Osteoporotic Vertebral Fractures

OSTEO+6
Start date: December 2007
Phase: Phase 4
Study type: Interventional

This study aims to compare two treatments in subacute (more than 6 week duration) non-traumatic (usually osteoporotic) vertebral fractures. The two treatments are the following: 1. Vertebroplasty consisting in the percutaneous injection into the fractured vertebra of polymethylmetacrylate cement (the cement used to fix prosthesis in joint replacement) through a posterior route through the vertebral pedicles under radiological guidance. 2. Balloon Kyphoplasty which consists of placing through a percutaneous posterior approach under radiological guidance, into the fractured vertebra a balloon which is inflated with fluid and creates a cavity. This may restore part of the vertebral height loss due to the fracture. In addition, after balloon deflation, polymethylmetacrylate cement is injected with low pressure into the created cavity to fix fracture reduction. The study will indicate if balloon kyphoplasty is able to restore vertebral height of the fractured vertebra better than vertebroplasty.

NCT ID: NCT00749060 Completed - Clinical trials for Osteoporotic Vertebral Fracture

Comparison of Balloon Kyphoplasty, Vertebroplasty and Conservative Management in Acute Osteoporotic Vertebral Fractures

OSTEO-6
Start date: December 2007
Phase: N/A
Study type: Interventional

This study aims to compare three treatments in recent (less than 6 week duration) non-traumatic ( usually osteoporotic) vertebral fractures.

NCT ID: NCT00679978 Completed - Rheumatic Diseases Clinical Trials

Vertebral Fracture and Osteonecrosis Associated With High-dose Glucocorticoid

Start date: January 2001
Phase: Phase 4
Study type: Observational

Osteoporotic vertebral fracture (VF) and osteonecrosis of the femoral head (OFH) are major concerns in patients with systemic rheumatic diseases treated with high-dose glucocorticoids (GCs). The investigators examined and compared the incidence and risk factors of VF with those of OFH in patients who had recently received high-dose GC therapy to clarify the relationship between these two complications.

NCT ID: NCT00638768 Completed - Osteoporosis Clinical Trials

Effectiveness of Physiotherapy for Osteoporotic Spinal Fracture

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

The aim of this pilot study was to determine the effect of physiotherapy on impairments and health-related quality of life in people with a painful osteoporotic spinal fracture. It is hypothesised that physiotherapy will reduce impairments and improve quality of life in this patient group.

NCT ID: NCT00616694 Completed - Osteoporosis Clinical Trials

Impact of Vertebral Fracture Knowledge on Persistence in Subjects Taking Glucocorticoid Therapy

ACTIVATE
Start date: July 2002
Phase: Phase 4
Study type: Interventional

To evaluate the effect of subject knowledge of their disease status on persistence in subjects receiving Actonel 5 mg daily over a 12-month period for the prevention and treatment of GIO.

NCT ID: NCT00463905 Completed - Osteoporosis Clinical Trials

Evaluation of the Impact of a Case-finding Strategy for Vertebral Fractures

COSHIBA
Start date: October 2007
Phase: N/A
Study type: Interventional

Postmenopausal women with vertebral fractures (VFs) represent an important target for secondary fracture prevention, but few of these patients come for clinical attention. Recent evidence suggests that screening postmenopausal women for clinical risk factors like height loss and fracture risk identifies those at high risk of prevalent VFs who should be referred for diagnostic X-rays, a strategy which is likely to prove cost effective. However, before being applied at a United Kingdom (UK)-wide level, it needs to be established that use of this strategy improves secondary fracture prevention, and that these benefits are achieved in a cost-effective manner. To examine these questions, a randomised-controlled-trial will be performed in which women aged 65-80 from general practitioner (GP)-practices in the intervention group will be invited for risk factor assessment, followed by referral for thoracolumbar X-ray where appropriate. The primary outcome will be a change in bisphosphonate or other drug prescribing between the intervention and control arms after six months.