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Spinal Cord Injuries clinical trials

View clinical trials related to Spinal Cord Injuries.

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NCT ID: NCT00693563 Completed - Spinal Cord Injury Clinical Trials

Scheduled Telephone Intervention for Individuals With Spinal Cord Injury and Their Families

SCILink
Start date: August 2007
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate whether scheduled telephone intervention with individuals with spinal cord injury (SCI) and their caregivers in the first year following discharge from acute inpatient rehabilitation will reduce rehospitalizations and emergency room visits as well as improve adjustment to SCI.

NCT ID: NCT00667966 Completed - Spinal Cord Injury Clinical Trials

Assess Efficacy in Subjects With Traumatic Spinal Cord Injury

LEMDE
Start date: July 2005
Phase: Phase 4
Study type: Interventional

Assess efficacy of Vardenafil in patients with traumatic spinal cord injury

NCT ID: NCT00663663 Completed - Multiple Sclerosis Clinical Trials

Telephone Intervention for Pain Study (TIPS)

TIPS
Start date: September 2009
Phase: N/A
Study type: Interventional

Treatments teaching people how to manage pain have been used to treat chronic pain in the general population. The purpose of this study is to see if these treatments delivered over the telephone can benefit persons with multiple sclerosis, spinal cord injury or an acquired amputation. Specifically, we want to determine if these treatments can help reduce the negative consequences that pain often causes in terms of a person's mood, daily activities, and enjoyment of life. We are also interested in finding out if these treatments decrease a person's pain.

NCT ID: NCT00662207 Completed - Clinical trials for Urinary Incontinence

Two Devices for Reflex Voiding Following Spinal Cord Injury

Start date: October 2008
Phase: Phase 1
Study type: Interventional

The purpose of this investigation is to evaluate methods in spinal cord injured individuals to improve reflex urination. Anal dilation will be investigated to reduce high urethral resistance and a vibrator on the patient's bottom will be tested to induce more sustained bladder contractions for better bladder emptying.

NCT ID: NCT00656149 Completed - Spinal Cord Injury Clinical Trials

In-home Telerehabilitation for Quadriplegic Hand Function

SCI-IHT
Start date: May 2007
Phase: Phase 2/Phase 3
Study type: Interventional

1. To evaluate improvements in hand function in stable, cervical spinal cord injured (SCI) subjects treated with functional electrical stimulation (FES)-assisted exercise; 2. To compare the information obtained from existing qualitative and quantitative hand function tests with newly developed tests of sensorimotor performance. Hypotheses: 1. the performance of tasks representative of activities of daily living (ADL) will improve with daily tele-supervised exercise of the affected hand. 2. The improvements will be greater in one exercise protocol than the other, the protocols being a) FES-assisted exercise on a workstation, b) cyclical FES, weight training and precision tasks. 3. Scores derived from quantitative data obtained from sensors on the workstation will correlate with the qualitative scores of the primary outcome measure, the ARAT hand function test.

NCT ID: NCT00654680 Completed - Clinical trials for Erectile Dysfunction

Evaluating the Efficacy and Safety of Vardenafil in Patients Erectile Dysfunction Solely Secondary to Spinal Cord Injury

Start date: October 2002
Phase: Phase 3
Study type: Interventional

Investigate efficacy and safety of Vardenafil in patients with spinal cord injury

NCT ID: NCT00654082 Completed - Spinal Cord Injury Clinical Trials

A Study Evaluating the Efficacy and Safety of Sildenafil in Men With Traumatic Spinal Cord Injury and Erectile Dysfunction

Start date: September 2002
Phase: Phase 4
Study type: Interventional

To demonstrate the efficacy, safety and tolerability of sildenafil administered orally, as required, approximately 1 hour prior to sexual activity to men with erectile dysfunction (ED) associated with spinal cord injury (SCI), as well as its effects on the quality of life (QoL) of these patients.

NCT ID: NCT00652262 Completed - Spinal Cord Injury Clinical Trials

BAY38-9456 - Supportive Trial for Spinal Injury

Start date: March 2004
Phase: Phase 3
Study type: Interventional

BAY 38-9456 10 mg and 20 mg can be given as safe and efficacious medications to patients with spinal cord injury suffering from erectile dysfunction, and that erectile dysfunction can be improved by uptitration to BAY 38-9456 20 mg when the treatment with 10 mg is not sufficiently effective

NCT ID: NCT00645567 Completed - Spinal Cord Injury Clinical Trials

Biomechanics of Wheelchair Transfers

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

This is a laboratory-based study to evaluate the risk of shoulder injury associated with transfers between wheelchair and vehicle in persons with spinal cord injury. Four new devices will be compared against an unassisted transfer.

NCT ID: NCT00628446 Completed - Heart Diseases Clinical Trials

Coronary Heart Disease as Measured by Coronary Calcium Score Among Individuals With Chronic Traumatic Spinal Cord Injury

Start date: September 2007
Phase:
Study type: Observational

This study includes male subjects age 45 to 70, who have sustained a traumatic Spinal Cord Injury (SCI) at least 10 years prior. Subjects will be interviewed for demographic data, including heart disease risk factors. A blood test for cholesterol levels will be drawn. A CT scan of arteries of the heart will be performed to determine the presence of coronary calcium, a marker of subclinical Coronary Heart Disease. Scoring of Coronary Calcium or Coronary Calcium Score (CCS) is automated by the CT scanner. Each subject's Framingham Risk Score will be calculated; This is an individuals 10 year risk of having a Coronary Heart Disease event (significant symptoms). In addition, it will be determined if subjects are being treated for diagnosed dyslipidemia (high cholesterol) according to the National Cholesterol Educational Program (NCEP) guidelines. The proposed pilot study aims to better understand the problem of Coronary Heart Disease in individuals with Spinal Cord Injury, specifically CCS in SCI, when compared to the general population.