Physiopathology, Diagnosis and Therapy of Primary Cephalalgia and Adaptive Disorders

Sponsor
IRCCS National Neurological Institute "C. Mondino" Foundation (Other)
Overall Status
Completed
CT.gov ID
NCT04696510
Collaborator
(none)
15
1
27.5
0.5

Study Details

Study Description

Brief Summary

The main aim of the present pilot study is to prove the possibility to use the Nitroglycerin (NTG) model to describe the pathophysiology of headache using task-free advanced Magnetic Resonance Imaging (MRI) techniques, in order to depict the static changes of the ictal and inter-ictal phase of migraine attacks vs the pain free state in healthy subjects and to compare that with the spontaneous headache attack experienced by chronic migraineurs.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Resting state functional magnetic resonance imaging (rs-fMRI) has depicted cyclical functional connectivity changes during the ictal and inter-ictal phase of the migraine attack. In this pilot study, Functional Connectivity (FC) changes during nitroglycerin (NTG) induced migraine attacks were assessed vs the pain-free condition in healthy subjects.

    To this end, subjects with episodic migraine (EM) without aura were enrolled. NTG-triggered a spontaneous-like migraine attack in the subjects. They underwent 4 rs-fMRI scan repetitions during different phases of the attack (baseline, prodromal, full blown, recovery phase) with a 3 Tesla MR scanner. According to the pain field literature, several regions of interests were studied, in particular the thalamic areas and the salience network (SN) were selected as primary areas of interest for the analyses. Subjects' rs-fMRI data were first processed with a seed-based correlation analysis (SCA) to assess the static changes in FC between the thalamus and the rest of the brain during the experiment. The wavelet coherence approach (WCA) were also applied to test the changes in time-in-phase coherence between the thalamus and the salience network (SN).

    Healthy subject were administered nitroglycerin as well and scanned at a pain free baseline and after 3 hours in order to compare the response.

    The rebound headache that followed acute drug withdrawal were used as a surrogate paradigm of spontaneous attack. Patients with chronic migraine and medication overuse were hospitalized for a supervised withdrawal program at the Mondino Foundation; during the program if they experienced a rebound headache attack, they were scanned with a rs-fMRI acquisition.

    The acquired imagines were analyzed with the same procedure regarding the evaluation of static and dynamic functional connectivity fluctuation.

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    15 participants
    Observational Model:
    Case-Control
    Time Perspective:
    Prospective
    Official Title:
    Biomarker Identification to Predict the Evolution of Migraine From an Episodic to a Chronic Condition
    Actual Study Start Date :
    Aug 31, 2018
    Actual Primary Completion Date :
    Mar 31, 2019
    Actual Study Completion Date :
    Dec 15, 2020

    Arms and Interventions

    Arm Intervention/Treatment
    Chronic migraineurs

    This group includes patients with chronic migraine.

    Control group

    This group includes healthy subjects.

    Episodic migraineurs

    This group includes patients with episodic migraine

    Outcome Measures

    Primary Outcome Measures

    1. Functional Connectivity (FC) changes [Up to 6 hours]

      Functional connectivity pattern of changes profiling the different condition of the migraine experience. To depict the static and dynamics changes of brain activity during a migraine attack; ii) To validate the use of the NTG-induced attacks paradigm as a reliable instrument combined with an fMRI approach to compare the induced vs the spontaneous attack; iii) To describe possible differences in brain activity between attacks in chronic and episodic migraineurs.

    Secondary Outcome Measures

    1. Magnetic Resonance Imaging (MRI) [Up to 6 hours]

      To acquire sufficient MRI to identify feature patterns that can profile patient's condition using machine learning (ML) and deep learning (DL) algorithms. This can be achieved by combining clinical, psychological, biological, neurophysiological and MRI-derived features into a multimodal multi-parametric approach suitable for patient's classification. The ML and DL approaches could also be adopted to predict chronification, as well as the response to a withdrawal program for medication overuse headache.

    2. Monthly migraine frequency (day/month) [Up to 6 hours]

      To acquire clinical data to identify feature patterns that can profile patient's condition using machine learning (ML) and deep learning (DL) algorithms.

    3. Disease duration (years) [Up to 6 hours]

      To acquire clinical data to identify feature patterns that can profile patient's condition using machine learning (ML) and deep learning (DL) algorithms.

    4. Nausea (number) [Up to 6 hours]

      As a feature of the migraine attack.To acquire clinical data to identify feature patterns that can profile patient's condition using machine learning (ML) and deep learning (DL) algorithms.

    5. Vomiting (number) [Up to 6 hours]

      As a feature of the migraine attack.To acquire clinical data to identify feature patterns that can profile patient's condition using machine learning (ML) and deep learning (DL) algorithms.

    6. Photophobia (number) [Up to 6 hours]

      As a feature of the migraine attack.To acquire clinical data to identify feature patterns that can profile patient's condition using machine learning (ML) and deep learning (DL) algorithms.

    7. Phonophobia (number) [Up to 6 hours]

      To acquire clinical data to identify feature patterns that can profile patient's condition using machine learning (ML) and deep learning (DL) algorithms.

    8. Aggravation by movement (number) [Up to 6 hours]

      As a feature of the migraine attack. To acquire clinical data to identify feature patterns that can profile patient's condition using machine learning (ML) and deep learning (DL) algorithms.

    9. Throbbing pain (number) [Up to 6 hours]

      As a feature of the migraine attack. To acquire clinical data to identify feature patterns that can profile patient's condition using machine learning (ML) and deep learning (DL) algorithms.

    10. Abortive medication (number of intake/month) [Up to 6 hours]

      To acquire clinical data to identify feature patterns that can profile patient's condition using machine learning (ML) and deep learning (DL) algorithms.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 60 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes

    Episodic migraineurs

    Inclusion Criteria:
    • age between 18-60 years;

    • diagnosis of episodic migraine without aura developed before the age of 50;

    • no current prophylactic treatment for migraine prevention;

    • chronic migraineurs with medication overuse according to the ICHDIII criteria

    Exclusion Criteria:
    • chronic or medication-overuse headache or cluster headache diagnosis;

    • any chronic pain condition or disorders other than migraine;

    • an alleged diagnosis of major psychiatric disorders such as depression, bipolar affective disorder and schizophrenia;

    • a diagnosis of tension type headache with a frequency of more than 5 days per month;

    • any cardiovascular diseases in which the NTG use could be contraindicated;

    • blood pressure hypotension, closed angle glaucoma, anaemia;

    • women in child bearing, breast feeding; continuous use of benzodiazepines;

    • any neuroradiological pathological findings at a previous MRI scan of the head.

    Chronic migraineurs

    Inclusion Criteria:
    • age between 18-60 years;

    • diagnosis of migraine without aura developed before the age of 50 according to the ICHD III criteria;

    • currently chronic migraineurs with medication overuse according to The International Classification of Headache Disorders 3rd edition (ICHDIII) criteria.

    Exclusion Criteria:
    • any chronic pain condition or disorders other than migraine;

    • an alleged diagnosis of major psychiatric disorders such as depression, bipolar affective disorder and schizophrenia;

    • a diagnosis of tension type headache with a frequency of more than 5 days per month;

    • any cardiovascular diseases in which the NTG use could be contraindicated;

    • blood pressure hypotension, closed angle glaucoma, anaemia; women in child bearing, breast feeding;

    • continuous use of benzodiazepines;

    • any neuroradiological pathological findings at a previous MRI scan of the head.

    Healthy subjects

    Inclusion Criteria:
    • age between 18-60 years;

    • overall good clinical condition, no neurological findings at the physical examination.

    Exclusion criteria:
    • history of episodic or chronic or medication-overuse headache or cluster headache diagnosis according to the International Chronic Headache Disease (ICHD) III criteria;

    • any chronic pain condition or disorders other than migraine;

    • an alleged diagnosis of major psychiatric disorders such as depression, bipolar affective disorder and schizophrenia;

    • a diagnosis of tension type headache with a frequency of more than 5 days per month;

    • any cardiovascular diseases in which the NTG use could be contraindicated;

    • blood pressure hypotension, closed angle glaucoma, anaemia;

    • women in child bearing, breast feeding;

    • continuous use of benzodiazepines;

    • any neuroradiological pathological findings at the baseline MRI scan of the head.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Headache Science Center Pavia Italy 27100

    Sponsors and Collaborators

    • IRCCS National Neurological Institute "C. Mondino" Foundation

    Investigators

    • Principal Investigator: Cristina Tassorelli, Prof, IRCCS Mondino Foundation, Pavia

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    IRCCS National Neurological Institute "C. Mondino" Foundation
    ClinicalTrials.gov Identifier:
    NCT04696510
    Other Study ID Numbers:
    • IMAGO2020
    First Posted:
    Jan 6, 2021
    Last Update Posted:
    Jan 6, 2021
    Last Verified:
    Nov 1, 2020
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by IRCCS National Neurological Institute "C. Mondino" Foundation
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jan 6, 2021