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Spinal Fracture clinical trials

View clinical trials related to Spinal Fracture.

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NCT ID: NCT03359941 Terminated - Fractures, Bone Clinical Trials

Acupuncture Treatment for Vertebral Compression Fracture

Start date: February 1, 2016
Phase: N/A
Study type: Interventional

Patients with vertebral compression fractures (VCF) may experience pain, limitation of daily activities, and various complications (e.g., insomnia, constipation, urinary infection, depression, diminished quality of life). Objective: This study aims to evaluate the effectiveness, safety and feasibility of acupuncture treatments to achieve pain relief and functional recovery in patients with VCF.

NCT ID: NCT03316703 Recruiting - Spinal Fracture Clinical Trials

Surgical Treatment of the Thoracolumbar Spine Fractures.

Start date: May 9, 2018
Phase: N/A
Study type: Interventional

The thoracolumbar segment fractures are the most frequent along the spine, and surgical treatment is indicated in unstable fractures. Surgical treatment has been performed through the posterior fixation pedicle fixation systems, and where necessary complemented by decompression of the spinal arthrodesis and previous channel. Surgical treatment has been performed by conventional open approach through the posterior incision on the midline, and detachment and removal of paraspinal muscles to access the posterior vertebral elements. The percutaneous minimally invasive surgery was introduced in the context of spinal surgery to reduce the morbidity associated with conventional open approach. It has been reported the lowest bleeding intra- and postoperative period, less pain, shorter hospital stay, rehabilitation and return to work faster with less use of minimally invasive percutaneous approach of the spine. However, predominates in the literature of clinical case reports and few prospective and randomized clinical trials. The performance of prospective randomized clinical trials have been required for the evaluation of the benefits of minimally invasive surgery in the treatment of the thoracolumbar spine fractures. The objective of the study is to compare the surgical treatment of fractures of the thoracolumbar spine using the conventional open approach or minimally invasive percutaneous approach to the stabilization of the vertebral segment affected, and using similar type of pedicle spinal fixation system. Patients will be evaluated in the preoperative, postoperative, 1,2,3,6,12 and 24 months by parameters related to the perioperative (intraoperative bleeding, surgery time), clinical (VAS, SF-36, HADS, EQ-5D-5L), images (radiographs and computed tomography). The study results will impact the guidelines of the surgical treatment of thoracolumbar spine fractures and may indicate the advantages or disadvantages of using surgery through conventional open approach to minimally invasive percutaneous surgery.

NCT ID: NCT03312998 Not yet recruiting - SPINAL Fracture Clinical Trials

Incidence of Metal Failure During First Year Following Transpedicular Screws Fixation of Dorsolumbar Spine Fracture

Start date: December 1, 2017
Phase: N/A
Study type: Interventional

Recording incidence of metal failure in transpedicular screws fixation of dorsal umbra spine fracture during first year follow up

NCT ID: NCT03272243 Completed - SPINAL Fracture Clinical Trials

Short Segment vs Long Segment Fixation in Traumatic Dorsolumbar Spine Fractures

Start date: February 1, 2012
Phase: N/A
Study type: Interventional

A prospective study included 91 patients, who had single level thoracolumbar fracture with Cobb's angle ≤ 25⁰, underwent posterior fixation. Forty four patients underwent short segment fixation with screws into the index level, and 47 patients underwent long segment fixation with skipped index level. The angle of correction, pain, and neurological state were regularly assessed

NCT ID: NCT03269851 Completed - SPINAL Fracture Clinical Trials

Parameters of Neurological Deficit After Thoracolumbar Fractures

Start date: November 1, 2018
Phase:
Study type: Observational

To detect Radiological parameters affecting neurological injury after thoracolumbar spinal fractures.

NCT ID: NCT03253952 Recruiting - SPINAL Fracture Clinical Trials

A Study of Autonomic Dynamic Dysfunction to Predict Infections After Spinal Cord Injury.

Start date: September 29, 2017
Phase:
Study type: Observational

The study is designed to investigate whether autonomic shifts (dysautonomia, sympatho-vagal instability) that develop after SCI have value in predicting SCI-associated infections (SCI-AI). SCI-AI impair outcomes by (1) reducing the intrinsic neurological recovery potential and (2) increasing mortality. Heart Rate Variability (HRV) data will be tracked in both the time and frequency domains to discriminate between the relative contribution of sympathetic and parasympathetic innervation to changes in HRV. The ability to predict infections will enable novel treatments thereby reducing infection-associated mortality and improving neurological and functional outcomes.

NCT ID: NCT02252185 Completed - Spinal Stenosis Clinical Trials

A Clinical Study of a Spine Fusion System in Vertebral Body Fusion Surgery

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

The primary objective of this study is to demonstrate that the efficacy and safety of Spine fusion system manufactured in China is no inferior than imported product.

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: NCT00343252 Completed - Back Pain Clinical Trials

Effect of Teriparatide Compared to Risedronate on Back Pain in Women With a Spine Fracture Caused by Osteoporosis

Start date: June 2006
Phase: Phase 3
Study type: Interventional

The purpose of the study is to determine if daily teriparatide reduces back pain more effectively than weekly risedronate in women with osteoporosis who have chronic back pain due to a spinal bone fracture.