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Headache clinical trials

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NCT ID: NCT04490798 Completed - Chronic Pain Clinical Trials

Effectiveness of Acupuncture Clinical Pathway

ACUPATHWAY
Start date: June 12, 2020
Phase:
Study type: Observational

The study will be described the development and implementation of the Clinical pathway (CPW) for acupuncture treatment in the management of patients with some chronic pain conditions. The effectiveness of this CPW will be explored in this study through retrospective analysis of clinical outcomes after administration of acupuncture treatment summarised in the guidelines.

NCT ID: NCT04467398 Recruiting - Clinical trials for Trigeminal Neuralgia

Incidence of Intravascular (IV) Injection During Trigeminal Nerve Blocks

Start date: July 20, 2020
Phase:
Study type: Observational [Patient Registry]

The purpose of this study is to investigate the incidence of intravascular injection during trigeminal nerve blocks.

NCT ID: NCT04454541 Completed - Clinical trials for Cervicogenic Headache

Efficacy of Ultrasound-Guided Multifidus Cervicis Plan Block Vs Greater Occipital Nerve Block for Cervicogenic Headache

UBLOC
Start date: May 1, 2019
Phase: N/A
Study type: Interventional

Background: Cervicogenic headache (CH) described as a chronic hemi-cranial pain resulted from a disorder of the cervical spine and its anatomic structures innervated by the C1, C2, and C3 cervical spinal nerves. Traditionally noninvasive and invasive techniques were used for treatment. Greater occipital nerve block is the most frequent peripheral nerve block invasive technique used for the management of cervicogenic headache Objectives: The study was done to compare the efficacy of two different techniques: multifidus cervicus plan block and greater occipital nerve block in treatment of refractory cervicogenic headache using ultrasound guided. Patients and Methods: sixty patients with cervicogenic headache were recruited and diagnosed according to ICHD-ш Beta version. Divided into two group, one for greater occipital nerve block and the other for multifidus cervicis plane block with ultrasound guided.

NCT ID: NCT04452929 Recruiting - Migraine Clinical Trials

The Effect of Anti-calcitonin Gene-related Peptide (CGRP) Receptor Antibodies on the Headache Inducing Properties of CGRP and Cilostazol in Migraine Patients

Start date: July 22, 2020
Phase: N/A
Study type: Interventional

A randomized, double-blind, placebo-controlled, parallel study to investigate the effect of erenumab in calcitonin-gene related peptide and cilostazol experimental models of migraine in humans. Followed by a 6-month open-label extension.

NCT ID: NCT04439409 Terminated - Cluster Headache Clinical Trials

Variability of the Autonomic Nervous System (ANS) During Cluster Headache (CH).

AVASNA
Start date: August 19, 2020
Phase:
Study type: Observational

Cluster Headache (CH) is associated with ipsilateral vegetative signs, related to parasympathetic system hyperactivity and/or signs of sympathetic hypoactivity. The precise mechanism of Cluster Headache (CH) is still unknown. The question is whether these dysautonomic disorders are simply secondary to the Cluster Headache (CH) process or whether they are the triggering factor.

NCT ID: NCT04410536 Recruiting - Clinical trials for Migraine, Hemicrania

Home Detox in Medication Overuse Headache (MOH) During Covid-19 Emergency

MOHC
Start date: June 15, 2020
Phase: N/A
Study type: Interventional

Medication Overuse Headache (MOH) is a disabling condition that affects the 2% of migraine population. Medication overuse (MO) makes this condition very difficult to treat. The literature of the last decades confirm the efficacy of withdrawal for patients with medication overuse, but it is also confirmed that patients have to be carefully followed after withdrawal to avoid relapses and to improve the clinical benefit of the therapeutic approach. Clinical results can be improved when traditional therapies are combined with behavioral approaches in particular mindfulness, that help patient to become more conscious about their symptoms and able to manage pain without medication. As the emergency situation due to the Corona-virus pandemic phenomenon in Italy, the regular clinical practice adopted for patients with CM-MO has changed in the last weeks: patients cannot come to the hospital for the withdrawal iv therapy and for regular follow up as the reduced mobility due to the emergency in particular in the Lombardia region, but all over Italy. So the investigators propose a pilot study to enforce the application of a Home-program for the withdrawal procedure for patients and the use of technology like smartphone and video calls so that patients can continue to be followed in their therapeutic process by using behavioral support and mindfulness practice. Patients will perform the withdrawal program at home, by oral administration of therapies, with specific instructions and education. Also the information for behavioral approach and mindfulness practice will be given, to use every day at home. Daily standardized mindfulness sessions of 12 minutes on their smartphone will be combined with weekly video-call to evaluate the clinical condition and to encourage the use strategies for pain management. Face-to-face visits at the follow up every three months will be scheduled. This modality will allow the patients to continue their therapeutic process and to be regularly followed during the one year after withdrawal.

NCT ID: NCT04409977 Recruiting - Cluster Headache Clinical Trials

Circadian Changes of the Hypothalamic Activity in Patients Suffering From Cluster Headache

Start date: June 26, 2019
Phase:
Study type: Observational

Cluster headache attacks do not occur randomly throughout the day, but have a clear circadian rhythmicity. The aim of this study is to investigate circadian changes of the brain, the autonomic nervous system and pain processing systems.

NCT ID: NCT04406259 Recruiting - Cluster Headache Clinical Trials

Atrioventricular Block and Cluster Headache (SEVA)

SEVA
Start date: November 2, 2020
Phase: Phase 4
Study type: Interventional

Verapamil is a calcium channel blocker widely used to treat cardiovascular diseases however it is also the first line treatment in the prevention of cluster headaches. In France, its prescription in that indication is based on compliance with the Temporary Recommendation for Use (RTU) that insists on the possible the cardiac side effects that can occur as the doses required for cluster headache are significantly higher than the doses used in cardiology.

NCT ID: NCT04401878 Completed - Clinical trials for Post-Dural Puncture Headache

SGB in Management of Patients With PDPH Using TCD

Start date: May 24, 2020
Phase: N/A
Study type: Interventional

This study aims to investigate the ability of SPGB in the management of PDPH. Transcranial Doppler is also used as an measure to assess the block success by detecting the variability in the cerebral hemodynamics before and after the block.

NCT ID: NCT04401501 Completed - Headache Clinical Trials

Effects of Manual Therapy on the Upper Cervical Spine Combined With Exercise vs Isolated Exercise in Patients With Cervicogenic Headache.

Start date: June 1, 2020
Phase: N/A
Study type: Interventional

Cervicogenic headache is defined as unilateral headache associated with neck pain. Effect of manual translatoric therapy of the upper cervical spine associated with cervical exercises in these patients is currently unknown. Our aim was to determine if adding manual therapy to an exercise and home-exercise program improved effects on symptoms and function in short- and mid-term in patients with cervicogenic headache. A randomized controlled study will be conducted with 40 subjects with cervicogenic headache. Each group will receive four 20-minute sessions weekly and a home-exercise program. Upper cervical flexion, flexion-rotation test, Impact Headache Test-6 (HIT-6), headache intensity, craniocervical flexion test, pain pressure thresholds and Global Rating of Change (GROC)-Scale will be assessed at end of the intervention, at 3- and at 6-month follow-ups.