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Headache clinical trials

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NCT ID: NCT00531895 Completed - Major Depression Clinical Trials

An Open Trial of Duloxetine on Comorbid Major Depression and Chronic Headache

Start date: April 2006
Phase: Phase 4
Study type: Interventional

Background: Although major depression and chronic headache are strongly associated, there is insufficient evidence on the use of antidepressants for this specific comorbidity. This trial aimed to investigate the efficiency and tolerability of duloxetine for this indication. Methods: Thirty outpatients of our clinic, with DSM-IV major depression and concurrent primary chronic headache (chronic migraine, chronic tension-type headache or both), 18-55 years, were recruited from April 2006 to March 2007, if they scored >21 on the Montgomery-Äsberg Depression Scale (MADRS) and had no other significant clinical condition. Subjects received duloxetine 60 mg/day for 8 weeks. MADRS scores and a visual analog pain scale (VAS) were the co-primary outcome measures. WHO quality of life scale (WHOQoL BREF) scores and headache days/week were secondary outcome measures.Conclusion: In this preliminary open trial, duloxetine 60 mg/day was effective, fast acting and well tolerated for the treatment of comorbid major depression and chronic headache.

NCT ID: NCT00530517 Completed - Migraine Headache Clinical Trials

A Study on the Usability of the Needle-free Intraject® System in Adult Patients During Acute Migraine Attack

Start date: September 2007
Phase: Phase 2
Study type: Interventional

Intraject is a needle-free, single use, disposable, subcutaneous delivery system pre-filled with 6mg Sumatriptan to be used by patients to treat acute migraine treatment. Study participation will last one month and include 2 doctor visits and 2-4 phone calls.

NCT ID: NCT00520156 Not yet recruiting - Clinical trials for Obstructive Sleep Apnea

Analysis of the Prevalence and Characteristics of Concomitant Sleep and Headache Disorders, and the Efficacy of CPAP Treatment for Headache Among Those Patients Diagnosed With Obstructive Sleep Apnea

Start date: August 2007
Phase: N/A
Study type: Observational

There is a well-documented but poorly understood relationship between headache disorders (e.g. migraine, cluster headaches, awakening headaches, etc.) and sleep disorders. One hypothesis includes an underlying disorder known as obstructive sleep apnea (OSA) with low overnight oxygen saturations and possibly elevated carbon dioxide levels which result in awakening headache. Bruxism, or grinding of the teeth, has also been anecdotally associated with headache. The converse of these arguments is that the patient may have a primary headache disorder, for example migraine, leading to disordered sleep patterns or insomnia. The true relationship between the two, as alluded above, is unknown. The actual prevalence of the two disorders occurring simultaneously is not known. There have been several small, retrospective studies which have attempted to evaluate this relationship. One of these studies evaluated those patients diagnosed with OSA who were given the standard of care therapy - continuous positive airway pressure (CPAP) - and found that headaches among these patients were improved after using CPAP. Again, this was a small, retrospective study. We propose a study whereby patients who are referred for polysomnography (PSG, or "sleep study") are consented, then surveyed on the presence or absence of headache. A brief questionnaire is followed up with a more detailed questionnaire to characterize whether this headache that the patient has is truly a headache disorder. Following the survey and PSG, the patient's sleep study parameters are evaluated to see whether there are certain correlations between what has been recorded and the particular headache disorder present. Lastly, if the patient was diagnosed with OSA and fitted with a CPAP device, the patient will be queried several weeks later to evaluate whether there was improvement or cessation of the headache disorder.

NCT ID: NCT00510172 Recruiting - Migraine Clinical Trials

Migraine Inducing Effects and Changes in Brain Haemodynamics of PGI2

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

We hypothesised that intravenous infusion of PGI2 induced headache or migraine and cranial vasodilatation in migraineurs.

NCT ID: NCT00487578 Terminated - Clinical trials for Post Traumatic Headache

Naratriptan for the Treatment of Post Traumatic Headache Associated With Cognitive Dysfunction

Start date: October 2006
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine whether naratriptan, a medication approved for treatment of migraine, is effective in the treatment of post traumatic headache associated with cognitive dysfunction.

NCT ID: NCT00458770 Terminated - Cluster Headache Clinical Trials

Study of Hypothalamic Metabolism in Spontaneous Cluster Headache Attacks

Start date: May 2009
Phase: N/A
Study type: Interventional

Cluster headache is characterized by unilateral excruciating head pain and autonomic dysfunction. Hypothalamic overactivity was observed in nitrate-induced cluster-headache and in only one case of spontaneous cluster headache 'Sprenger et al, 2004). This prompted the application of hypothalamic deep brain stimulation. The aim of this data is to precise the localisation of the hypothalamic activation.

NCT ID: NCT00457496 Completed - Neck Pain Clinical Trials

Effectiveness of a Cognitive and Physical Intervention to Reduce Head and Muscle Pain in Working Communities

Start date: March 2005
Phase: Phase 3
Study type: Interventional

The primary purpose of this study is to evaluate the effectiveness of a workplace cognitive and physical program (Intervention), in reducing the frequency of head and neck pain

NCT ID: NCT00450060 Recruiting - Headache Clinical Trials

Juvenile Postlumbar Puncture Headache After Puncture With Needles With Quincke Tip or With Sprotte Tip

Start date: January 2007
Phase: N/A
Study type: Interventional

The purpose of this study is to compare postlumbar puncture complaints as headache or backache after lumbar puncture with needles with Quincke design or with Sprotte design in children and adolescents.

NCT ID: NCT00449787 Completed - Migraine Clinical Trials

Comparing Naproxen to Sumatriptan for Emergency Headache Patients

HEDNet2
Start date: March 2007
Phase: Phase 4
Study type: Interventional

2/3 of patients discharged from an emergency department after treatment for an acute headache will still be bothered by headache within 24 hours of emergency department (ED) treatment. The goal of this study is to compare two medications, naproxen and sumatriptan, to determine which is better for the treatment of recurrent headache within 24 hours of emergency department discharge.

NCT ID: NCT00434083 Completed - Migraine Headaches Clinical Trials

To Evaluate the Safety and Efficacy of Trexima in the Acute Treatment of Migrane Headaches

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

- to demonstrate the superiority of Trexima (combination of sumatriptan as the succinate 85 mg and naproxen sodium 500 mg) versus placebo in the acute treatment of migraine - to demonstrate the superiority of Trexima versus the individual components (sumatriptan as the succinate 85 mg and naproxen sodium 500 mg), and - to evaluate the safety of the Trexima.