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Post-concussive Syndrome clinical trials

View clinical trials related to Post-concussive Syndrome.

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NCT ID: NCT02690584 Completed - Brain Injuries Clinical Trials

Metacognitive Therapy for Post-concussive Symptoms After Mild Traumatic Brain Injury

Start date: March 2016
Phase: N/A
Study type: Interventional

The purpose of this open trial is to investigate the feasibility, acceptability, and effect of metacognitive therapy in patients with prolonged post-concussive symptoms after mild traumatic brain injury.

NCT ID: NCT02643836 Withdrawn - Concussion Clinical Trials

Pulsed Electromagnetic Field (PEMF) Therapy for Post-Concussive Syndrome

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

The objectives are to evaluate impact of Pulsed electromagnetic field (PEMF) therapy on patients with Post-Concussive Syndrome with Rivermead Post Concussion Symptom Questionnaire (RPQ) as a primary outcome, followed by fatigue and mood as second and tertiary outcomes respectively. The investigators will also investigate brain tissue activity and oxygenation by evaluating brain wave activity via non-invasive quantitative electroencephalogram and near infrared spectroscopy testing pre and post study to better understand the metabolic effect of the PEMF intervention. The investigators hypothesize that the PEMF treatment will have an effect on improvement of brain metabolism as measured by Near Infrared Spectroscopy which will in turn assist with improvement of the chronic symptoms of cognitive deficits, mood and fatigue as related to Post-Concussive Syndrome.

NCT ID: NCT01762475 Completed - Clinical trials for Traumatic Brain Injury

Sildenafil for Cerebrovascular Dysfunction in Chronic Traumatic Brain Injury.

Start date: January 2013
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether sildenafil (Viagra®) is effective in improving cerebral blood flow and cerebrovascular reactivity inpatients who have persistent symptoms at least 6 months after a traumatic brain injury (TBI).

NCT ID: NCT01315379 Recruiting - Clinical trials for Traumatic Brain Injury

Psychological Treatment for Children Suffering From Post Traumatic Stress Symptoms and Mild Traumatic Brain Injury

TBI
Start date: April 2011
Phase: N/A
Study type: Observational

The purpose of this study is to determine whether Prolonged Exposure Therapy (PE)is effective in the treatment of post-traumatic stress symptoms in children and adolescents with mild traumatic brain injury (m-TBI) due to motor vehicle accident.

NCT ID: NCT01220713 Completed - Clinical trials for Mild Traumatic Brain Injury

Hyperbaric Oxygen Therapy (HBO2T) for Post-Concussive Symptoms (PSC) After Mild Traumatic Brain Injury (mTBI)

HBOT
Start date: June 2010
Phase: Phase 2
Study type: Interventional

The goal of this research is to serve as a demonstration project to determine the tolerability of individuals with persistent post-concussive symptoms from combat-related mild TBI (traumatic brain injury), identify dose-finding for HBO2 (Hyperbaric Oxygen) therapy, and determine the efficacy of HBO2 therapy.

NCT ID: NCT01101724 Completed - Clinical trials for Mild Traumatic Brain Injury

Effect of Early Rest on Recovery From Pediatric Concussion

Start date: April 2010
Phase: N/A
Study type: Interventional

The purpose of this study is to find out if strict rest for 5 days helps children get better after concussion.

NCT ID: NCT00653029 Terminated - Clinical trials for Post Concussive Syndrome

An fMRI Study of Attention and Effort After Concussion

Start date: October 2006
Phase: N/A
Study type: Observational

Approximately 1.1 million people a year suffer a mild traumatic brain injury (MTBI), or concussion, in the United States. Although most MTBI patients fully recover, as many as 28% have physical, cognitive, and/or emotional symptoms up to 6 months post-injury. When symptoms persist past three months, it is known as post-concussion syndrome (PCS). The cause of PCS is unknown, as structural neuroimaging and neuropsychological (NP) testing results are often normal. However, recent functional magnetic resonance imaging (fMRI) research in concussed adults showed differences in brain activity compared to controls on working memory tasks, despite normal structural MRI and neuropsychological findings. We propose improving this research by assessing brain activation patterns during simple versus complex attention and working memory tasks in 10 concussed adults via fMRI. This will be the first study to examine brain activation patterns associated with the degree of effort applied to testing, a factor known to confound interpretation of NP test performance. Validated computerized measures of selective attention (Modified Stroop Interference Task), working memory (n-back), and effort (Green's Medical Symptom Validity Test; MSVT) will be used. Ten paid controls will be used for comparative purposes. We hypothesize that concussed patients will show less brain activation than controls on complex versus simple working memory tasks and that activation patterns in concussed patients will generally be lower in those with suboptimal effort. We will also characterize self-reported emotional and physical symptoms in the PCS patients, which has not been done in prior fMRI research with this population.

NCT ID: NCT00237705 Recruiting - Clinical trials for Post Concussive Syndrome

Intravenous Metoclopramide for the Treatment of Post Concussive Headache: a Randomized Placebo Controlled Trial

Start date: May 2004
Phase: N/A
Study type: Interventional

Concussion is defined as any temporary disturbance in brain function following a blow to the head. It may not involve a loss of consciousness and usually results in a post concussive headache (PCH) immediately after the injury. Between 30 and 50 percent of patients with concussion will develop postconcussive syndrome (PCS) consisting of symptoms such as headache, and a variety of other debilitating symptoms lasting several weeks to months. The objective of this study is to determine if metoclopramide, a drug commonly used in the treatment of migraine headache, will be effective in relieving PCH and in preventing PCS. Eligible patients will have a history of a concussion resulting in headache within the past 24 hours. Patients will rate their pain on a standard scale before and after being treated with one or two intravenous doses of either metoclopramide or saltwater placebo. They will be contacted by telephone 1, 4 and 8 weeks later in order to determine if they have developed the postconcussive syndrome.