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Headache clinical trials

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NCT ID: NCT00663585 Completed - Clinical trials for Chronic Daily Headache

Intensive Meditation and Migraines: Effects on Health and Well Being

Start date: April 2008
Phase: N/A
Study type: Interventional

Participants completing training in intensive meditation and continuing frequent practice for one year would experience reduced frequency, duration and severity of headaches along with improved awareness of the triggers of their symptoms, improved quality of life and mental health, improved heart rate variability, and reduced inflammation.

NCT ID: NCT00662935 Completed - Cluster Headache Clinical Trials

Evaluation of Efficacity and Safety of Deep Brain Stimulation (DBS) in Chronic and Treatment-Resistant Cluster Headache(CH)

Start date: May 2005
Phase: N/A
Study type: Interventional

The aim of this study is to evaluate the efficacy and safety of deep brain stimulation (DBS) in chronic and treatment-resistant CH. Inclusion criteria are: patients with chronic CH (>3years), with daily attack and non response to adequate treatment. Electrodes are implanted stereotactically in the postero-inferior hypothalamus. In this crossover, randomized, placebo-controlled double-blinded study, the efficacy of DBS is evaluated using comparison of two one-month sequences: one with stimulation "on" and the other with stimulation "off" (placebo sequence). Efficacy is defined as ≥50% decrease of weekly frequency of CH attacks. After the randomized period, long-term efficacy and safety are evaluated after one year of stimulation in open conditions.

NCT ID: NCT00642564 Completed - Epilepsy Clinical Trials

Study on Migraine and Headache in Epileptic Patients

Start date: February 2008
Phase: Phase 4
Study type: Observational

The purpose of this study is to collect data from patients who are diagnosed with epilepsy and are followed up in epilepsy clinics.

NCT ID: NCT00632606 Withdrawn - Headache Clinical Trials

MgSO4 vs Metoclopramide for Headache in Pregnant Women

MagHead
Start date: August 2008
Phase: Phase 2/Phase 3
Study type: Interventional

The study will compare effectiveness of intravenous magnesium sulfate to that of intravenous metoclopramide (Reglan®) for acute headache in pregnant women. We will randomize pregnant women who present to our emergency department with chief complaint of headache to magnesium sulfate 2 grams intravenously or metoclopramide 10 mg intravenously; both groups will receive acetaminophen (Tylenol®) 1 gram orally and normal saline 1 liter intravenously. Headaches are common during pregnancy, related to hormonal changes, altered sleep patterns and psychosocial stressors. Common medications for headache such as non-steroidal antiinflammatories or triptans are typically avoided during pregnancy due to concern for fetal effects. Women, and their physicians, are often uncertain regarding available medication options with justifiable safety profiles during pregnancy.

NCT ID: NCT00617318 Completed - Influenza Clinical Trials

Pomegranate Products for Prevention of Common Cold

Start date: January 2007
Phase: Phase 3
Study type: Interventional

Pomegranate has a long history of use in folk medicine. There is vast data on the health benefits of pomegranate fruit and juice. Multiple studies have established the strong antioxidative effects of pomegranate polyphenols (primarily the ellagitannin punicalagin) and their health effects. A vast number of animal and human clinical studies have provided evidence on effect of pomegranate products on improving blood lipid profile, reducing blood pressure, improving endothelial function, anti-tumor activity, and its anti-atherosclerotic activity. We studied the protective effect of a pomegranate concentrate (POM Flu and Cold Formula®) in decreasing the incidence and duration of influenza-like illnesses and common cold among healthy adults.

NCT ID: NCT00610428 Completed - Clinical trials for Migraine Headache, With or Without Aura

Staccato Prochlorperazine in Migraine (in Clinic)

Start date: March 2005
Phase: Phase 2
Study type: Interventional

Development of Staccato Prochlorperazine for the treatment of migraine headache.

NCT ID: NCT00600717 Enrolling by invitation - Healthy Clinical Trials

Clinical Applications of High-Frequency Oscillations

HFOs
Start date: November 1, 2000
Phase:
Study type: Observational

The objective of this study is to use high-frequency brain signals (HFBS) to localize functional brain areas and to characterize HFBS epilepsy, migraine and other brain disorders. We hope to build the world's first high-frequency MEG/MEG/ECoG/SEEG database for the developing brain. HFBS include high-gamma activation/oscillations, high-frequency oscillations (HFOs), ripples, fast ripples, and very high frequency oscillations (VHFOs) in the brain. To reach the goals, we have developed several new MEG/EEG methods: (1) accumulated spectrogram; (2) accumulated source imaging; (3)frequency encoded source imaging; (4) multi-frequency analysis; (5)artificial intelligence detection of HFOs; (6) Neural network analysis (Graph Theory); and (7) others (e.g. ICA, virtual sensors).

NCT ID: NCT00580307 Terminated - Headache Clinical Trials

Rhinogenic Headache Improvement After Nasal Operation

RHINO
Start date: December 2007
Phase: N/A
Study type: Interventional

Objective: To determine the efficacy of surgical correction of intranasal mucosal contact points in improving quality of life and decreasing medication use in patients with rhinogenic headaches.

NCT ID: NCT00564408 Completed - Headache Clinical Trials

Carbachols Headache-inducing Effect and Changes in Cerebral Blood Flow in Migraine Patients

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

The purpose of this study is to test if carbachol infusion induces headache in migraine subjects as well as intra- and extra-cerebral vasodilatation.

NCT ID: NCT00551980 Completed - Migraine Clinical Trials

The Efficacy of a Cognitive and Physical Intervention to Reduce Head and Muscle Pain in a Working Community

Start date: October 2007
Phase: Phase 3
Study type: Interventional

This study is a controlled, cluster randomised, interventional trial to evaluate the effectiveness of a workplace cognitive and physical program (Intervention), in reducing the frequency of head and neck pain in an extensive working population.