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Anodal Transcranial Direct Stimulation (tDCS) for the Treatment of Chronic Cluster Headache (ANODECCH)

Primary Purpose

Chronic Cluster Headache

Status
Completed
Phase
Phase 2
Locations
Belgium
Study Type
Interventional
Intervention
tDCS
Sponsored by
University of Liege
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Chronic Cluster Headache

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Main inclusion criteria for CCH: preventive CH therapy stable for a least 2 months, retrospective 4-week headache baseline diary showing at least 4 attacks/week on average

Exclusion Criteria:

  • No other significant medical or psychiatric disease.

Sites / Locations

  • CHR Citadelle

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Cefaly tDCS

Arm Description

Sponge-electrodes (5 x 7 cm) will be postioned at Fz (anode) and over the spinous process of C7 (cathode). Stimulation intensity will be set to 2 mA.

Outcomes

Primary Outcome Measures

Reduction of weekly cluster headache attack frequency during and following tDCS treatment in CCH patients.
Analysis of the headache diary

Secondary Outcome Measures

reduction of intensity of CH attacks
Analysis of the headache diary
reduction of duration of CH attacks
Analysis of the headache diary
reduction of acute medication intake
Analysis of the headache diary
modification of the nociceptive blink reflex
modification of pain thresholds
using quantitative sensory testing

Full Information

First Posted
May 27, 2015
Last Updated
December 6, 2016
Sponsor
University of Liege
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1. Study Identification

Unique Protocol Identification Number
NCT02462395
Brief Title
Anodal Transcranial Direct Stimulation (tDCS) for the Treatment of Chronic Cluster Headache
Acronym
ANODECCH
Official Title
Anodal Transcranial Direct Stimulation (tDCS) of the Anterior Cingulate Gyrus for the Treatment of Chronic Cluster Headache: a Pilot Trial.
Study Type
Interventional

2. Study Status

Record Verification Date
December 2016
Overall Recruitment Status
Completed
Study Start Date
September 2014 (undefined)
Primary Completion Date
September 2016 (Actual)
Study Completion Date
September 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Liege

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Cluster headache is a primary headache that chiefly affects young men, and is less common than migraine. This disease can have devastating consequences due to the pain intensity (it is also called "suicide headache"), to the side effects of the drug preventive therapies, and to the resistance of some subtypes of the headache to all existing medications. Recent studies suggest that cluster headache could be associated with a decrease of the activity of frontal areas involved in descending pain control, in particular the subgenual anterior cingulate cortex. The aim of this pilot study is to activate these areas with a non-invasive neurostimulation technique, called transcranial direct current stimulation, as a preventive treatment for cluster headache sufferers.
Detailed Description
Cluster headache affects 0.1%-0.25% of the general population, but its prevalence may be underestimated. It is a primary headache disorder with a higher prevalence in young males, characterized by attacks of severe unilateral periorbital/temporal pain with autonomic symptoms (ie lacrimation, nasal congestion, eyelid edema, Horner's…) and agitation, lasting 15 to 180 minutes and occurring periodically in bouts (clusters) in about 90% of patients (episodic cluster headache or ECH, ICHD-III criteria 3.1.1).In 10% of patients there is no sustained spontaneous remission for long periods, which defines chronic cluster headache (CCH, ICHD-III criteria 3.1.2). The pathophysiology of cluster headache is not completely understood, but neuroimaging studies clearly suggest that activation of the ipsilateral postero-ventral hypothalamus plays a seminal role during the attack. Recent findings suggest that prefrontal areas may be dysfunctioning in cluster headache patients. The investigator shave shown in CCH patients that the beneficial effects of ONS are associated with activation of the subgenual anterior cingulate cortex, an area responsible for descending pain-control. Transcranial direct current stimulation (tDCS) allows activating the underlying cortex and connected subcortical structures under the anode or inhibiting them under the cathode. tDCS was used as a therapeutic strategy in various neurological disorders, chronic pain disorders and depression. Because of its non-invasiveness, It is of particular interest in primary headaches where various brain areas are known to function abnormally even between headache attacks. It has been tested in migraine but not in cluster headache. In a recent study, the investigators have shown that anodal tDCS over the visual cortex is able to modify visual evoked potentials in healthy volunteers and migraineurs, and after a 2-month treatment of 2 weekly sessions to significantly decrease attack frequency in episodic migraine. CCH patients will have to apply the neurostimulation outside of an attack every day for 20 minutes during 4 to 8 weeks. Adherence to the treatment will be evaluated by monitoring the time during which the device is switched on via an in-built software.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Cluster Headache

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
32 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Cefaly tDCS
Arm Type
Experimental
Arm Description
Sponge-electrodes (5 x 7 cm) will be postioned at Fz (anode) and over the spinous process of C7 (cathode). Stimulation intensity will be set to 2 mA.
Intervention Type
Device
Intervention Name(s)
tDCS
Other Intervention Name(s)
tDCS Cefaly Technology°.
Intervention Description
Sponge-electrodes (5 x 7 cm) will be postioned at Fz (anode) and over the spinous process of C7 (cathode). Stimulation intensity will be set to 2 mA. A first group of CCH patients will have to apply the neurostimulation outside of an attack every day for 20 minutes during 4 weeks. A second group will use the tDCS device everyday for 8 weeks. Adherence to the treatment will be evaluated by monitoring the time during which the device is switched on via an in-built software.
Primary Outcome Measure Information:
Title
Reduction of weekly cluster headache attack frequency during and following tDCS treatment in CCH patients.
Description
Analysis of the headache diary
Time Frame
4 to 8 weeks
Secondary Outcome Measure Information:
Title
reduction of intensity of CH attacks
Description
Analysis of the headache diary
Time Frame
4 to 8 weeks
Title
reduction of duration of CH attacks
Description
Analysis of the headache diary
Time Frame
4 to 8 weeks
Title
reduction of acute medication intake
Description
Analysis of the headache diary
Time Frame
4 to 8 weeks
Title
modification of the nociceptive blink reflex
Time Frame
4 to 8 weeks
Title
modification of pain thresholds
Description
using quantitative sensory testing
Time Frame
4 to 8 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Main inclusion criteria for CCH: preventive CH therapy stable for a least 2 months, retrospective 4-week headache baseline diary showing at least 4 attacks/week on average Exclusion Criteria: No other significant medical or psychiatric disease.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Delphine Magis, MD
Organizational Affiliation
University of Liege
Official's Role
Principal Investigator
Facility Information:
Facility Name
CHR Citadelle
City
Liege
ZIP/Postal Code
4000
Country
Belgium

12. IPD Sharing Statement

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Anodal Transcranial Direct Stimulation (tDCS) for the Treatment of Chronic Cluster Headache

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