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Headache clinical trials

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NCT ID: NCT01408069 Withdrawn - Clinical trials for Tensional-type Headache

Non-Inferiority Comparison of Migrane® Versus Parcel ® For Treatment of Tensional Cephaleia

Start date: n/a
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the non-inferiority clinical efficacy of two different associations of drugs in the treatment of patients diagnosed with tensional-type headache in accordance with International Headache Society guidelines.

NCT ID: NCT01390324 Withdrawn - Migraine Clinical Trials

Efficacy and Safety of a Fixed-dose Combination of Naratriptan and Naproxen in Acute Treatment of Migraine

Atenéia
Start date: December 2011
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine whether a fixed-dose combination of naratriptan + naproxen is effective compared each monotherapy for the acute treatment of migraine.

NCT ID: NCT01347684 Withdrawn - Clinical trials for Tension-type Headache

Assessing the Effectiveness of Two Treatment Strategies for Tension-type Headache

Start date: April 2012
Phase: Phase 3
Study type: Interventional

The primary aim of the pilot data proposal is to compare usual care (medications) versus multi-disciplinary treatment in temporomandibular disorder (TMD) patients.

NCT ID: NCT01306266 Withdrawn - Clinical trials for Chronic Post-traumatic Headache

Study of Rizatriptan in the Treatment of Acute Attacks of Post-traumatic Headache in U.S. Military Troops

Maxalt
Start date: February 2011
Phase: N/A
Study type: Interventional

The purpose of the study is to determine the effectiveness of rizatriptan for treating attacks of chronic post-traumatic headache.

NCT ID: NCT00990574 Withdrawn - Hypotension Clinical Trials

A Study Comparing Two Spinal Techniques for for Cesarean Delivery Anesthesia

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

The purpose of this study is to compare single shot versus sequential bolus spinal technique via a catheter in patients undergoing Cesarean Section. We aim to determine which technique results in less blood pressure reduction and subsequent vasopressor use. Other study endpoints include the incidence of maternal post dural puncture headaches and nausea and vomiting. In addition blood and CSF will be collected to see if biochemical mediators are related to wound hyperalgesia and healing.

NCT ID: NCT00732108 Withdrawn - Migraine Clinical Trials

Is Topiramate Effective in Treating Dizziness in Patient's With Migraine-Associated Dizziness

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

The purpose of this study is to determine whether topiramate effective in treating dizziness symptoms that are associated with migraine headaches.

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: NCT00373074 Withdrawn - Clinical trials for Post-Lumbar Puncture Headache

Epidural Blood Patch on the Resolution of Postdural Puncture Headache (PDPH)

Start date: September 2006
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to address the question, "What is the volume of blood for injection at epidural blood patch that most effectively relieves post-dural puncture headache?"

NCT ID: NCT00258791 Withdrawn - Mental Disorders Clinical Trials

Effects of Pretreatment With Ibuprofen in Post-Electroconvulsive Therapy (ECT) Headache

Start date: January 2012
Phase: N/A
Study type: Interventional

The purpose of the study is to determine whether ibuprofen reduces post-ECT headache or reduces its severity.