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Spinal Cord Diseases clinical trials

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NCT ID: NCT04319679 Terminated - Pain Clinical Trials

ESWT for UE Pain in Patients With Cervical Spinal Cord Injury

Start date: June 5, 2020
Phase: N/A
Study type: Interventional

This study aimed to investigate the efficacy and safety of extracorporeal shockwave therapy (ESWT) for upper extremity pain related to spasticity in patients with spinal cord injury.

NCT ID: NCT04265560 Terminated - Clinical trials for Spinal Cord Injuries

Progressive Resistance Training in Acute Spinal Cord Injury

Start date: November 1, 2019
Phase: N/A
Study type: Interventional

Muscle weakness is one of the most common and debilitating symptoms following a Spinal Cord Injury (SCI). Strength training is recommended as an effective means to increase muscular strength and improve function for individuals with long term SCI. In contrast, the strength training guidance for those with a recent (<1 year) SCI is lacking. Therefore, this study aims to investigate the feasibility of a method of upper limb strengthening - Progressive Resistance Training (PRT) and its impact upon muscle strength and function.

NCT ID: NCT03191526 Terminated - Clinical trials for HTLV-1 Associated Myelopathy

A Study of KW-0761 in Subjects With HTLV-1 Associated Myelopathy (HAM)

Start date: May 22, 2017
Phase: Phase 3
Study type: Interventional

The objective of this study is to assess the efficacy and safety of KW-0761 after intravenous injections in subjects with HTLV-1 associated myelopathy (HAM) in Japan.

NCT ID: NCT03062657 Terminated - Radiculopathy Clinical Trials

An Investigation of the Metal Concentration in Patients Implanted With the PRESTIGE LP™ Cervical Disc at Two Contiguous Levels in the Cervical Spine

Start date: June 6, 2018
Phase: N/A
Study type: Interventional

This clinical study will assess the metal concentrations present in the blood serum of patients who receive surgical treatment with the PRESTIGE LP™ Cervical Disc at two contiguous cervical levels from C3-C7. The information obtained from this clinical investigation will be used to support the post market surveillance for a PMA supplement for the PRESTIGE LP™ Cervical Disc implanted at two contiguous levels.

NCT ID: NCT02974673 Terminated - Clinical trials for Spinal Cord Diseases

Pilot Study of Ejaculatory Dyssynergia by Electronic Microsensors of Sphincters

EDGE
Start date: February 15, 2017
Phase: N/A
Study type: Interventional

The objective of this research is to study the sphincter activity during ejaculation in patients with spinal cord injury in order to detect an ejaculatory dyssynergia. For this purpose, using a catheter the protocol plans to measure the sphincter pressures during ejaculation. Moreover, cardiovascular parameters will be measured continuously during the ejaculatory test.

NCT ID: NCT02758899 Terminated - Diabetes Clinical Trials

Diabetes and Glycosylation in Cervical Spondylosis

Start date: March 2014
Phase:
Study type: Observational

The purpose of this study is to determine the relevant significance of diabetes on cervical disc degeneration, and correlate diabetic control (HgbA1C) with disc glycosylation profile in patients undergoing anterior cervical discectomy and fusion for cervical spondylosis. Additionally, to compare the level of degenerative cervical disc glycosylation in patients with and without diabetes. Hypothesis: Patients with diabetes and degenerative cervical disc disease have higher levels of disc tissue glycosylation, and higher levels of glycosylation are correlated with poor outcomes.

NCT ID: NCT02403453 Terminated - Radiculopathy Clinical Trials

RHINE™ Cervical Disc Clinical Study: A Prospective Observational Study for Patients Requiring 1-2 Level C-spine Surgery

Start date: January 2016
Phase:
Study type: Observational

A Prospective, open label, multi-center observational study of patients requiring surgical treatment at one or two (contiguous) cervical spine levels. The primary objectives of the RHINE Cervical Disc study are to: obtain operative data and feedback on surgical instruments and surgical technique; confirm device performance in terms of clinical and radiographic outcomes; confirm device performance in terms of safety and to collect original data to be compared to published reports of the performance of comparable motion-sparing devices, as well as clinical outcomes of fusion devices.

NCT ID: NCT02248701 Terminated - Clinical trials for Spinal Cord Injuries

Testosterone Plus Finasteride Treatment After Spinal Cord Injury

Start date: April 27, 2017
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether testosterone plus finasteride treatment will improve musculoskeletal health, neuromuscular function, body composition, and metabolic health in hypogonadal men who have experienced ambulatory dysfunction subsequent to incomplete spinal cord injury. The investigators hypothesize that this treatment will improve bone mineral density, enhance muscle size and muscle function, and improve body composition, without causing prostate enlargement.

NCT ID: NCT02068547 Terminated - Radiculopathy Clinical Trials

Bone Marrow Aspirate Concentration in Posterior Cervical Fusion

BMAC
Start date: February 2014
Phase: N/A
Study type: Interventional

The purpose of this research is to test if that combining bone marrow aspirate (removing bone marrow with a needle) concentration with locally harvested (collected) autograft (patient's own bone from another part of the body) for use as the bone graft results in equal rates of a successful procedure (fusion), as compared to current best practice in high-risk patients undergoing posterior cervical fusion. Hypothesis: Bone marrow aspirate concentration combined with locally harvested autograft results in equivalent rates of bony fusion, as compared to current best practice in high-risk patients undergoing posterior cervical decompression and fusion.

NCT ID: NCT01561755 Terminated - Clinical trials for HIV-associated Myelopathy

A Double-Blind, Placebo Controlled Study of Intravenous Immunoglobulin for HIV-Associated Myelopathy

Start date: February 2012
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine whether Intravenous Immunoglobulin (IVIG) is an effective treatment for HIV associated myelopathy.