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Migraine Disorders clinical trials

View clinical trials related to Migraine Disorders.

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NCT ID: NCT00329459 Completed - Migraine Disorders Clinical Trials

Treximet (Sumatriptan/Naproxen Sodium), Formerly Known as TREXIMA, for Menstrual Migraine in Women With Dysmenorrhea

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

This study was designed to determine efficacy of TREXIMA compared to placebo for the treatment of a menstrual migraine.

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: NCT00311662 Completed - Clinical trials for Migraine Without Aura

Efficacy and Tolerability of Tonabersat in the Prophylaxis of Migraine Headache

Start date: April 2006
Phase: Phase 2
Study type: Interventional

Overall trial objectives: - Can treatment with tonabersat reduce the number of days with a migraine headache in patients who suffer from frequent migraine attacks - How well tolerated is treatment with tonabersat The study is based on the hypothesis that the unique mechanism of action of tonabersat will inhibit some of the early events in the generation of migraine and so be effective as prophylactic treatment

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: NCT00297336 Completed - Migraine Disorders Clinical Trials

An Observational Study Evaluating the Safety of Topiramate for the Prevention of Migraine

Start date: March 2005
Phase: N/A
Study type: Observational

A 6-month, observational, post authorization safety study for the collection and evaluation of additional safety data on topiramate as a prophylactic treatment for migraines in adult patients. According to current European and international guidelines the safety and efficacy of drugs will be continuously monitored even after their approval and market circulation.The applicable methods of monitoring include: Observational studies, voluntarily reported adverse events, clinical trials of IV phase and Post Authorization Safety Studies ( PASS). Post Authorization Safety Studies (PASS) during the use of a product are a significant source of information regarding the action of the drug or a therapeutic method under the circumstances of every day clinical practice.

NCT ID: NCT00293657 Completed - Headache (Migraine) Clinical Trials

Study of Lornoxicam or Placebo for Acute Treatment of the Headache of Migraine.

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

To determine whether a single dose of intravenous lornoxicam is superior to intravenous placebo for the acute treatment of moderate or severe headache associated with a single migraine attack in patients with a history of migraine. Two-thirds of patients in this study will receive a single dose of intravenous lornoxicam (8mg or 16 mg) and one-third of patients will receive a single dose of an intravenous placebo.

NCT ID: NCT00287781 Completed - Migraine Headache Clinical Trials

A Double Blind Randomized Controlled of Placebo and Nebulized Lidocaine for Migraine Headache

Start date: January 2002
Phase: N/A
Study type: Interventional

Migraine headaches have previously been shown to be responsive to intranasal lidocaine in a small study. Using a nebulizer to administer the drug would improve the feasibility of using the treatment. It would also spare the patient narcotics with their attendant side effects. Because of the potential for placebo effect a placebo control is necessary in this study.