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Migraine Disorders clinical trials

View clinical trials related to Migraine Disorders.

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NCT ID: NCT03555214 Completed - Migraine Clinical Trials

Efficacy of Manual Therapy for the Treatment of Migraine.

MT-Migraine
Start date: June 30, 2018
Phase: N/A
Study type: Interventional

Introduction According to the World Health Organization (WHO) at least 47% of adults have suffered from headache in the last year. The headache is not only painful but also disabling, it can be accompanied by social and personal problems, with a decrease in the quality of life and with economic losses. Migraine affects a large number of people and, if the predisposing factors are not controlled, it can become chronic. Once the chronification point of migraine has arrived, it seriously affects the quality of life of people, both in the workplace, social and leisure. objective Perform the application of a manual therapy treatment based on protocols that include techniques already proven to improve different areas of impact in patients with migraine. To evaluate various aspects, we will include the intensity of pain, the frequency of episodes, anxiety and depression, quality of life, etc ... and the limitations or disability that it produces. Material and methods This is a prospective, single-blind, randomized study with patients diagnosed with migraine. The sample will be distributed in 4 groups: a) experimental group that will receive combined treatment of soft tissues with techniques evidenced independently; b) Group that will receive independent structural techniques; c) the group that will receive the set of protocols a and b; d) and the placebo control group. Evaluation An initial assessment will be carried out, another at the end of the treatment and another follow-up one month after the end of the treatment. In addition, the evaluation will include the following instruments: the HDI scale (Headache Disability Inventory), the MIDAS scale (Migraine Disability Assessment Scale), the SF-36 Questionnaire, the EVA Scale (Visual-Analogue Scale), the HIT-6 Questionnaire, the BDI Questionnaire (Beck Inventory Depression), the STAI Questionnaire (The State-Trait Anxiety Inventory), the change perceived after the treatment and medication intake.

NCT ID: NCT03543254 Completed - Chronic Disease Clinical Trials

"Follow the Sutures". A New Procedure for Injection of Botulinum Toxin for Chronic Migraine

Start date: May 1, 2018
Phase: Phase 2
Study type: Interventional

There is no doubt that chronic migraine is a large public health problem, which is both disabling and costly. Many patients and headache doctors see Botulinum toxin (Botox) treatment as a big stride forward, but it is a problem that the effect has been shown in only one study, with a low therapeutic gain. For this reason, before this costly treatment is expanded to potentially several thousand patients in Norway, it would be highly desirable that 1) there is additional good scientific evidence for use of Botox , 2) a more effective treatment procedure is developed, 3) the potential for unblinding is reduced, and 4) the dose, number of injection sites and cost can be halved, and 5) the adverse effects are minimized. These may be the results of this pilot project where injections are given along the sutures, which can open up for a later randomized, blinded and controlled study.

NCT ID: NCT03536936 Completed - Migraine Clinical Trials

Oxygenation and Perfusion in Patients With Acute Migraine Attacks

OPAMA
Start date: January 1, 2010
Phase:
Study type: Observational

The aim of the study is to retrospectively evaluate brain perfusion and oxygenation in acute migraine attacks. Magnetic resonance perfusion and susceptibility weighted imaging are the technics to measure perfusion and oxygenation respectively.

NCT ID: NCT03526874 Completed - Episodic Migraine Clinical Trials

Occipital Blocks for Acute Migraine

Start date: April 3, 2019
Phase: Phase 3
Study type: Interventional

Migraine affects 10-28% of children and adolescents and yet 20-30% of patients are ineffectively treated with current oral and nasal options. Peripheral nerve blocks (PNBs), injections of local anesthetics over branches of the occipital and/or trigeminal nerves, have been associated with possible benefit for pediatric headaches in case series, and may be useful for both acute and preventive treatment of migraine for children who fail less invasive treatments. In fact, 80% of pediatric headache specialists reported using peripheral nerve blocks and carry low risk of serious side effects; however, peripheral nerve blocks have never been tested, formally, in a randomized pediatric trial. By applying a novel design that utilizes lidocaine cream as a run-in step, investigators intend to test the efficacy of the most commonly used peripheral nerve block, the greater occipital nerve (GON) block, as an acute treatment for pediatric migraine and determine whether lidocaine cream leads to successful blinding of the injection. The GON block is expected to prove effective in decreasing the pain of migraine, with lidocaine being superior to saline and lidocaine cream maintaining blinding.

NCT ID: NCT03521193 Completed - Migraine With Aura Clinical Trials

pLatelEts And MigRaine iN patEnt foRamen Ovale

LEARNER
Start date: February 15, 2018
Phase: N/A
Study type: Interventional

Migraine is a common, chronic neurovascular disorder characterized by attacks of severe headache, autonomic nervous system dysfunction and, in some patients, aura, and disabling neurological symptoms. Worldwide, migraine prevalence is as high as 18% in the general population. Increased frequency of patent foramen ovale (PFO) in migraineurs was first reported in 1998 in a case-control study. Since then, others have described a 60% prevalence of PFO in patients suffering from migraine with aura. The presence of a right-to-left shunt (RLS) is thought to be a potent trigger of migraine attacks, although the mechanism is unknown. Moreover, PFO closure has correlated with improved migraine symptoms in several retrospective uncontrolled studies. The aim of this single-center, prospective study is to assess the impact of PFO closure on migraine attacks over time together with evaluation of potential predictive risk factors.

NCT ID: NCT03499119 Completed - Migraine Clinical Trials

AMG 334 20160172 Pediatric Migraine PK Study.

Start date: May 4, 2018
Phase: Phase 1
Study type: Interventional

AMG 334 20160172 Pediatric Migraine PK Study.

NCT ID: NCT03490500 Completed - Hemorrhage Clinical Trials

Using the S100B Protein for Emergency Headache Management Care (S100)

S100
Start date: October 24, 2018
Phase:
Study type: Observational

The purpose of this study is to determine the negative predictive value of protein S100B that could exclude subarachnoid and intracranial haemorrhage for patient that present severe headache within the last 3 hours.

NCT ID: NCT03488563 Completed - Migraine Clinical Trials

Study to Determine Safety and Efficacy of B244 in Subjects With Episodic Migraine

Start date: March 30, 2018
Phase: Phase 2
Study type: Interventional

This is a prospective, randomized, vehicle-controlled, double-blind, multi-center study assessing the safety, tolerability, and efficacy of B244 delivered as an intranasal spray for preventive treatment in subjects with episodic migraine.

NCT ID: NCT03479060 Completed - Migraine Disorders Clinical Trials

Continue or Stop Applying Wet Cupping (Al-Hijamah) in Migraine

Start date: January 3, 2017
Phase: N/A
Study type: Interventional

This study evaluates the short and long-term effects of application of Wet Cupping Therapy (WCT) in the treatment of migraine headaches in adults.Half of the participants will continue WCT application and the other half will not.

NCT ID: NCT03472417 Completed - Migraine With Aura Clinical Trials

Partial Rebreathing in the Treatment of Migraine With Aura

CapnoMigra
Start date: November 2016
Phase: N/A
Study type: Interventional

A study to test the efficacy of a partial rebreathing device in treating and/or preventing migraine pain