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Migraine With Aura clinical trials

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NCT ID: NCT01741714 Completed - Clinical trials for Migraine Without Aura

Is Chiropractic Spinal Manipulative Therapy an Efficient Treatment Option for Migraine

Start date: February 2013
Phase: N/A
Study type: Interventional

This study will highlight and validate chiropractic spinal manipulative therapy (CSMT) for migraine. If the method proves to be effective, it will provide a new non-pharmacological treatment option for migraine. This is especially important since some migraineurs do not tolerate acute and/or prophylactic medicine, due to side effects or contraindications due to comorbidity of other diseases while others do not have effect. Thus, alternative treatment options are warranted. The applied methodology of the study will aim towards the highest possible research standards. This international study is a collaboration between Akershus University Hospital, University of Oslo (UiO), Norway and Macquarie University, Australia. The multidisciplinary professional backgrounds are physiotherapy, chiropractic and medicine. By increasing the methodological quality of the investigators research to a very high level, the investigators see the method to work as a guide to increase the quality of chiropractic research in the future, as previous randomized clinical trials (RCTs) of migraine used methodology showing room for improvement.

NCT ID: NCT01596166 Completed - Clinical trials for Migraine Without Aura

Intravenous Ketorolac and Metoclopramide for Pediatric Migraine in the Emergency Department

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

Migraine headaches are a common problem for children. When treatment at home fails, children may benefit from intravenous treatment administered in a hospital setting like the Emergency Department. Most treatments used however have only been tested in adults and the best treatment strategy for children is not always clear. The combination of more than one medication is frequently prescribed in Canadian Emergency Departments. The purpose of this study is to investigate whether the combination of ketorolac (an anti-inflammatory pain medication) and metoclopramide (an anti-nauseant that may also relieve migraine headaches) is better than metoclopramide by itself.

NCT ID: NCT01388699 Completed - Migraine With Aura Clinical Trials

Migraine and Endothelial Dysfunction

Start date: October 2010
Phase:
Study type: Observational

Recently, there is evidence that endothelial activation and dysfunction are associated with migraine, especially in female migraineurs with aura. Our objectives were to determine whether novel endothelial function markers are altered in female migraineurs with aura compared to age-matched controls.

NCT ID: NCT01257880 Completed - Migraine With Aura Clinical Trials

Comorbidities Associated With Migraine and Patent Foramen Ovale (CAMP)

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

The purpose of the study is to compare the rate of comorbidities associated with migraine aura (MA) between persons who have a large circulatory right-to-left shunt (RLS) and those who do not have RLS. Approximately 50% of individuals who have MA also have RLS due to patent foramen ovale (PFO). A PFO is an anatomical opening or flap between the upper chambers of the heart or atria that permits blood to pass from the right of the heart to the left side of the heart, without first going to the lungs to be filtered and oxygenated. Many health conditions and clinical syndromes including stroke, sleep apnea, and migraine have been linked to PFO. Although the mechanism is undetermined, it is hypothesized that microscopic blood clots and chemicals such as serotonin can pass through the PFO, travel to the brain, and cause headache and aura. Persons who have MA are at increased risk for stroke and transient ischemic attacks relative to people who do not have migraine. Migraine is also associated with the presence of white matter lesions in the brain and mild deficits in cognitive function associated with the posterior brain (vision, memory, processing speed). The risk of stroke in migraine is highest for women under the age of 45 who have aura and a high number of migraine headache days per month. No convincing evidence has been produced to explain the mechanism for the increased risk of ischemic stroke in migraine; however, increased platelet activation and aggregation is a plausible theory. We hypothesize that migraineurs with aura and large RLS (presumably due to a PFO) will be more likely to have sleep apnea, increased platelet activation, cognitive deficits, alterations in cerebral vasomotor function, and white matter lesions than migraineurs with aura who do not have PFO. The results of this exploratory study will generate hypotheses as to why subgroups of migraineurs have an increased risk of stroke and the impact of large PFO on comorbid conditions associated with migraine aura. Early identification of migraine subgroups with a constellation of clinical syndromes that increase risk of neurovascular diseases will allow initiation of preventive strategies that may ultimately reduce burden and improve the productive quality of life for these individuals.

NCT ID: NCT00920686 Completed - Migraine With Aura Clinical Trials

Study of NXN 188 for the Treatment of Migraine With Aura

Start date: June 2009
Phase: Phase 2
Study type: Interventional

NXN-188 Dihydrochloride is being developed as an immediate release oral product for the treatment of acute migraine. This study is being conducted to evaluate NXN-188 in subjects with a migraine history of aura.

NCT ID: NCT00884663 Completed - Chronic Migraine Clinical Trials

Candesartan Versus Propranolol for Migraine Prevention

Start date: April 2009
Phase: Phase 2/Phase 3
Study type: Interventional

The main aim of the present study is to compare candesartan with propranolol for migraine prophylaxis.

NCT ID: NCT00687947 Completed - Healthy Clinical Trials

Calcitonin Gene-related Peptide in Familial Hemiplegic Migraine (FHM) and Migraine With Aura (MA)

CGRP-2008
Start date: May 2008
Phase: N/A
Study type: Interventional

The aim of the present study is to explore the importance of migraine phenotype on the headache/migraine responses after CGRP in FHM-patients, MA-patients and healthy volunteers.

NCT ID: NCT00541736 Completed - Clinical trials for Familial Hemiplegic Migraine

Glyceryl-Trinitrate-Induced Headache in Patients With Familial Hemiplegic Migraine

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

The aim of the present study is to explore the importance of migraine genes on the headache/migraine responses after GTN in FHM-patients and healthy volunteers.

NCT ID: NCT00534560 Completed - Clinical trials for Migraine Without Aura

Dose Ranging Study of the Efficacy and Tolerability of Tonabersat in the Prophylaxis of Migraine Headache

TEMPUS
Start date: October 2007
Phase: Phase 2
Study type: Interventional

Primary objective: To investigate the efficacy and tolerability of two doses of tonabersat compared to placebo in the prophylaxis of migraine headache and to evaluate the longer term tolerability of tonabersat in an open label extension. Secondary objective(s): To obtain further data on the efficacy and dose response of tonabersat; To extend the safety and tolerability database of tonabersat; To obtain data on the pharmacokinetics of tonabersat.

NCT ID: NCT00471952 Completed - Clinical trials for Migraine Without Aura

Maxalt 10mg Plus Caffeine 75mg in the Acute Treatment of Migraine Headache

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

The purpose of this study is to evaluate the effect of rizatriptan, alone or combined with caffeine for treating acute attacks of migraine. Each subject will have 3 months to treat 3 acute migraine headache attacks. Each subject will be dispensed one box containing 3 packets of study medication labeled for Headache #1, Headache #2, or Headache #3. Each packet wil contain either Maxalt 10mg MLT or a Maxalt placebo (sugar pill), and a capsule containing either caffeine 75mg or a capsule containing placebo (sugar). One headache will be treated with a combination of Maxalt 10mg MLT and caffeine. Another headache will be treated with a combination of Maxalt 10mg MLT and a capsule containing placebo. A third headache will be treated with just placebo. Neither the subject, the study coordinator, or your study doctor will know in which order you will receive the three different treatments. This information is available in case of emergency.