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Migraine Attack Pain Phase Prediction Study

Prediction Study of the Pain Phase of Migraine Attacks in Patients With Episodic Migraine

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06459635
Acronym
PREDI-CRISIS
Enrollment
70
Registered
2024-06-14
Start date
2023-10-09
Completion date
2026-07-01
Last updated
2026-07-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Migraine, Migraine Disorders, Migraine Headache, Migraine With Aura, Migraine Without Aura

Keywords

Migraine, Headache, Predict, Prediction, headache prediction, predict headache, migraine prediction, predict migraine, migraine attacks, migraine attack, headache attack, migraine attack prediction, predict migraine attack, prediction algorithm, algorithm

Brief summary

The study of the ability to predict pain in a migraine attack, through premonitory symptoms and through an ambulatory monitoring device through real-time recording of hemodynamic variables, is one of the strategic lines of research of the unit. of Headaches at the Hospital de La Princesa since 2013 together with the Complutense and Polytechnic University of Madrid. Their results have been reflected in various publications (Pagán J, et al. Sensors 2015; Gago-Veiga AB, et al. J Pain Res 2018) and have promoted the creation of several invention patents.

Detailed description

Patients with episodic migraine will be recruited from the monographic headache clinics of the 7 centers participating in the study. These patients, for a maximum period of 2 months, must monitor their hemodynamic variables with a wearable device and record all the clinical characteristics of their migraine attacks. Subsequently, with these records, an individualized algorithm will be created for each patient that aims to predict the onset of the migraine attack.

Interventions

None listed

Sponsors

Fundación de Investigación Biomédica - Hospital Universitario de La Princesa
Lead SponsorOTHER
Hospital Vall d'Hebron
CollaboratorOTHER
Hospital Donostia
CollaboratorOTHER
Hospital Universitario Marqués de Valdecilla
CollaboratorOTHER
Hospital Clínico Universitario Lozano Blesa
CollaboratorOTHER
Hospital Universitario La Fe
CollaboratorOTHER
Hospital Clínico Universitario de Valladolid
CollaboratorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* Age between 15 years and 69 years. * Diagnosed with migraine by a headache neurologist and according to the criteria proposed by ICHD-3. * History of migraine of at least 1 year of evolution. * Normal neurological examination. * Have given your informed consent. * Be able to describe your clinical situation and the characteristics of your headache. * Have an average of 10 to 14 migraine days per month in the three months prior to inclusion (high-frequency episodic migraine). * User-level management capacity of "smartphone" type electronic devices. * Be able to complete two months of study follow-up.

Exclusion criteria

* Presence of another type of headache, with the exception of headache due to excessive use of analgesic medication. * Cognitive deficiency or any other pathology that may prevent or make it difficult for the patient to perform the study correctly. * Neurological focus in the examination. * Pregnancy or breastfeeding period. * Patients with known heart disease or bronchopathy, Sjögren\'s syndrome, diabetes mellitus, or hypo/hyperthyroidism. * Carriers of pacemakers, neurostimulators or any other electronic device that is considered to make the interpretation of biometric records difficult. * Anatomical problem that makes the use of the device impossible. * Patients in whom it is expected that a change in migraine preventive treatment or other usual treatment will be possible during the study period.

Design outcomes

Primary

MeasureTime frameDescription
Development of a prediction strategy for the onset of migraineFrom the beginning of treatment, which is the initial visit, to 2 months of follow-upDevelop a prediction strategy for the onset of migraine attacks in patients with episodic migraine, based on hemodynamic and clinical variables of migraine attacks.

Secondary

MeasureTime frameDescription
Posibility of predict the onset of pain in a migraine attackFrom the beginning of treatment, which is the initial visit, to 2 months of follow-upTo analyze whether it is possible to predict the onset of pain in a migraine attack, through ambulatory and non-invasive monitoring of physiological variables.
Individualized prediction algorithmFrom the beginning of treatment, which is the initial visit, to 2 months of follow-upImplement an individualized prediction algorithm that allows real-time prediction of the symptomatic phase of the migraine attack.
Effectiveness of the prediction modelFrom the beginning of treatment, which is the initial visit, to 2 months of follow-upMeasure the effectiveness of the prediction model both at the individual level and in a large group of patients.

Countries

Spain

Contacts

CONTACTAna Beatriz Gago Veiga
anabeatriz.gago@salud.madrid.org+34 915202416
CONTACTIris Fernández Lázaro
irisfdezlaz@gmail.com
PRINCIPAL_INVESTIGATORAna Beatriz Gago Veiga

Fundación de Investigación Biomédica - Hospital Universitario de La Princesa

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 3, 2026