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Headache clinical trials

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NCT ID: NCT02209155 Terminated - Clinical trials for Episodic Cluster Headache

R-Verapamil for the Prophylaxis of Episodic Cluster Headache

Start date: November 2013
Phase: Phase 2
Study type: Interventional

This is a double-blinded, randomized, parallel, placebo-controlled phase 2 study to evaluate the safety and efficacy of R-verapamil in the prophylaxis of episodic cluster headache.

NCT ID: NCT02195648 Completed - Clinical trials for Tension-Type Headache

Sub-occipital Muscle Inhibition in Tension Type Headache

TTH
Start date: February 2015
Phase: N/A
Study type: Interventional

The main objective of this study is to determine the effects caused in neck movement, neck pain, headache in patients with tension type headache and cervicogenic headache after application of sub-occipital muscle inhibition technique associated with interferential electrotherapy.

NCT ID: NCT02181205 Withdrawn - Clinical trials for Postdural Puncture Headache

Sphenopalatine Ganglion Block for Post-Dural Puncture Headache

Start date: November 2014
Phase: N/A
Study type: Interventional

The investigators are attempting to determine a less invasive method of treatment for postdural puncture headaches that can occur after regional anesthesia. The investigators will be evaluating the relief of headache with those subjects receiving treatment with a sphenopalatine ganglion block with bupivacaine versus placebo, evaluating the incidence of epidural blood patch, pain score of headache at 1 hour, then 24, 48, and 72 hours lower with post study treatment versus placebo, and potential side effects of those patients receiving study therapy as well as epidural blood patch.

NCT ID: NCT02177019 Completed - Frequent Headaches Clinical Trials

Assessment of a Personalized Health Care Intervention for Frequent Headache

Start date: August 2014
Phase: N/A
Study type: Interventional

The research project is a component of a mentored research career enhancement award. The purpose of the award is to help the PI and his collaborators prepare for future research grant opportunities through the Patient Centered Outcomes Research Institute (PCORI). The research project is a feasibility study with the following specific aims; 1) to assess outcomes associated with a personalized health plan for frequent headaches; 2) to identify measurable outcomes that are meaningful to patients with frequent headaches; and 3) to create a patient stakeholder group to inform patient-centered outcomes research for frequent headaches. Specific Aim #1 will be achieved by recruiting and enrolling 40 established patients at the Duke Family Medicine Center who have frequent headaches. The intervention consists of 3 study visits with the PI, 2 clinical consultations with subjects' established primary care provider at the Duke Pickens Family Medicine Center, and participation in 2 focus groups. Personalized health plans might consist of a combination of medical management, lifestyle changes, nutrition counseling, or other therapeutic modalities as appropriate. Data analysis will be descriptive; no formal hypotheses will be tested.

NCT ID: NCT02176655 Completed - Clinical trials for Delayed Alcohol Induced Headache

Pilot Study of VVD-101 for the Treatment of Delayed Alcohol-Induced Headaches

Start date: July 2014
Phase: Phase 2
Study type: Interventional

This study proposes to compare the efficacy of sumatriptan and aspirin to placebo as an acute abortive treatment for delayed alcohol induced headache in adult subjects.

NCT ID: NCT02170259 Completed - Clinical trials for Tension-type Headache

Manual Therapy for Tension Headache With Psychological Disorders

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

Introduction. Tension-type headache is a highly prevalent disorder with a significant socio-economic impact, affecting psychological aspects. This study aims to assess aspects pertaining to anxiety, depression, headache frequency and pain intensity. Subjects and methods. A clinical trial was conducted on 84 participants suffering from tension-type headache, divided into 4 groups, the mean age being 39.76 years (SD 11.38). The first group received suboccipital soft tissue treatment (ST); the second group was treated with articulatory technique (AT); the third group was applied a combination of both techniques (ST and AT) and a forth group which served as control group. Treatment sessions were administered during four weeks, with a post-treatment assessment, and follow-up after one month. The investigators conducted Repeated measures Analysis of Covariance (RM-MANCOVA) to evaluate the effect of treatment on between and within-subject conditions and their interaction on reported depression, anxiety, and headache pain frequency and intensity.

NCT ID: NCT02168764 Active, not recruiting - Clinical trials for Chronic Cluster Headache

Sphenopalatine Ganglion Stimulation for the Treatment of Chronic Cluster Headache

Start date: July 2014
Phase: N/A
Study type: Interventional

The primary objective of the study is to demonstrate the safety and efficacy of SPG stimulation with the ATI Neurostimulation System when used to treat acute cluster attacks in chronic cluster headache patients.

NCT ID: NCT02163993 Completed - Migraine Headache Clinical Trials

A Study of Galcanezumab (LY2951742) in Participants With Migraine Headache

Start date: July 7, 2014
Phase: Phase 2
Study type: Interventional

The main purpose of this study is to evaluate whether the study drug known as galcanezumab is safe and effective in the prevention of migraine headaches.

NCT ID: NCT02160535 Terminated - Clinical trials for Chronic Post Traumatic Headache

Treatment of Chronic Post-Traumatic Headache With OnabotulinumtoxinA

Start date: May 2014
Phase: Phase 3
Study type: Interventional

This study will provide evidence on whether the use of an FDA-approved drug therapy for the treatment of chronic migraine (OnabotulinumtoxinA) shows similar efficacy for treatment of chronic headaches caused by traumatic injury to the brain (TBI) from a direct hit to the head, or a fall, or a motor vehicle accident, or some other traumatic event.

NCT ID: NCT02150304 Completed - Clinical trials for Postdural Puncture Headache

Aminophylline Prophylaxis For Postdural Puncture Headache

Start date: January 2014
Phase: N/A
Study type: Observational

postdural puncture headache is a rare but serious complication of spinal anesthesia. many drugs were studied in prevention or treatment of that complication. However, there are limited numbers of trials about intravenous aminophylline for prevention. because of that we retrospectively aimed to investigate the effectiveness of aminophylline for postdural puncture headache in cesarean section.