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Migraine clinical trials

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NCT ID: NCT00335777 Completed - Migraine Clinical Trials

A Research Study Examining Migranal and Skin Sensitivity in Subjects With Migraine

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

This is a research study looking at Migranal (study drug) in the treatment of two migraine attacks in patients who have a history of cutaneous allodynia (pronounced q-tay-nee-us al-o-din-ee-a). Cutaneous allodynia is an increased skin sensitivity experienced during a headache. It has been noted in several studies that in patients with migraine, seventy nine percent of the patients experienced allodynia on the facial skin on the same side as the headache. Understanding more about allodynia may help us understand how the pain system works in migraine. This study will compare the differences, if any, in attacks treated early with study drug (at 1-hour from onset) and attacks treated later (at 4-hours). You will be asked to treat one attack early and one attack late for this study. If the first attack you treat is early (at 1 hour following onset of throbbing pain) then the second attack you treat should be late (at 4 hours following onset of throbbing pain). It is hoped that this study will provide information on the use of Migranal in subjects who have cutaneous allodynia. The results from this study may be used in the development of larger clinical trials. The study drug is a medication that is taken in the form of nasal spray.

NCT ID: NCT00330850 Completed - Migraine Clinical Trials

An Efficacy Study of a Single Dose Treatment of PRO-513 for Subjects Suffering a Migraine Attack

Start date: May 2006
Phase: Phase 3
Study type: Interventional

The purpose of the study is to show the efficacy of a single dose of PRO-513 for treating subjects suffering moderate pain form a migraine attack, with or without aura. The study is also intended to show the effectiveness of PRO-513 for associated symptoms of nausea, photophobia, and phonophobia due to a migraine attack.

NCT ID: NCT00329771 Completed - Migraine Clinical Trials

Research Study to Determine Sensitivity to Gentle Touch and Pressure During an Active Migraine Attack.

Start date: March 2006
Phase:
Study type: Observational

Cutaneous allodynia (pronounced q-tane-ee-us all-o-din-ee-a) is common in migraine. It is a heightened skin sensitivity during an active migraine attack. Migraine attacks in patients who experience allodynia are more difficult to treat. This study intends to collect and evaluate data on the phenomenon of allodynia in patients with episodic migraine during an actual attack. The results of this study may help clinicians better understand allodynia, thereby helping them diagnose and more effectively manage patients with migraine and allodynia.

NCT ID: NCT00329355 Completed - Migraine Clinical Trials

Menstrual Migraine Treatment With TREXIMET (Formerly Known as TREXIMA)

Start date: May 2006
Phase: Phase 3
Study type: Interventional

This study was designed to determine efficacy of TREXIMET (sumatriptan/naproxen sodium), formerly known as TREXIMA compared to placebo for the treatment of a menstrual migraine.

NCT ID: NCT00319137 Completed - Migraine Clinical Trials

An Adaptive Design Trial Of GW274150 In The Treatment Of Acute Migraine

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

Nitric oxide (NO) is likely to be involved in the development of migraine headache. Nitric oxide synthase (NOS) is an important chemical involved in the production of NO. Reduction of NOS, and therefore NO, may be an effective technique for the treatment of migraine headache. GW274150 is a highly selective inhibitor of NOS and offers the potential of anti-inflammatory activity in migraine through a novel mechanism of action. The intent of this study is to investigate the safety and efficacy of GW274150 for the acute treatment of migraine headache.

NCT ID: NCT00301665 Completed - Migraine Clinical Trials

Efficacy and Safety Study of Dysport® Used for Migraine Prophylaxis

Start date: February 2003
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the efficacy of botulinum toxin type A (Dysport®) injections into pericranial muscles compared to placebo to prevent migraine attacks.

NCT ID: NCT00300924 Completed - Migraine Clinical Trials

A Study of Rizatriptan Co-Administered With Acetaminophen for the Treatment of Acute Migraine

Start date: March 2006
Phase: Phase 3
Study type: Interventional

The purpose of this study is to test an experimental drug combination of two medications currently approved by the Food and Drug Administration (FDA) for migraine headache or other pain. These are called rizatriptan given with acetaminophen.

NCT ID: NCT00297375 Completed - Migraine Clinical Trials

A Study Comparing the Effectiveness and Safety of ULTRACET® (Tramadol HCl/Acetaminophen) Versus Placebo for the Treatment of Acute Pain From a Migraine Headache

Start date: April 2003
Phase: Phase 4
Study type: Interventional

The purpose of this study is to evaluate the effectiveness and safety of tramadol HCl/acetaminophen as a pain medication compared with placebo in the treatment of acute pain from a migraine headache. Although tramadol HCl/acetaminophen is approved to treat acute pain, it is not approved for the treatment of acute pain associated with migraine headache. The study hypothesis is that tramadol HCl/acetaminophen is safe and effective as a pain medication in the treatment of acute pain associated with a migraine headache.

NCT ID: NCT00286078 Completed - Migraine Clinical Trials

Treatment for Migraines With an Implantable Device

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

The purpose of this study is to evaluate the safety and effectiveness of an implantable device for difficult to treat migraine. There are a significant number of patients who have drug refractory migraine and alternative therapies are needed.

NCT ID: NCT00272896 Completed - Migraine Clinical Trials

Hemodynamic and Headache-Inducing Effect of Intravenous Vasoactive Intestinal Peptide in Migraineurs

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

We hypothesized that infusion of VIP may induce headache/migraine in migraineurs and that VIP-induced headache may be associated with dilation of intra- and extracranial vessels. To test this hypothesis, we performed a double blind placebo-controlled crossover study in migraineurs and studied the effect on headache and cerebral and systemic hemodynamic parameters.