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

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

Status
Terminated
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04439409
Acronym
AVASNA
Enrollment
19
Registered
2020-06-19
Start date
2020-08-19
Completion date
2021-12-15
Last updated
2023-10-27

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

Conditions

Cluster Headache

Keywords

Cluster Headache, Autonomic Nervous System, Seizure, Holter, Electrocardiogram, (LF/HF) ratio, Daytime seizure, Night seizure

Brief summary

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.

Detailed description

This study cares about the evolution of the Autonomic Nervous System (ANS) in Cluster Headache (CH) seizures. Patients will be offered Holter ECG to study the temporal relationships between changes in Autonomic Nervous System (ANS) activity during Headache (CH) seizures and changes in Autonomic Nervous System (ANS) activity before and after seizure treatment, using heart rate variability measurement. The hypothesis is that there would be an initial temporary sympathetic activation, followed quickly by parasympathetic hyperactivation and a return to a state of equilibrium.

Interventions

Holter electrocardiogram will be carried during 7 days to measure heart's electrical activity continuously.

Sponsors

Centre Hospitalier Universitaire de Saint Etienne
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patient over 18 years of age * Affiliated or entitled to a Social Security scheme * Resident in the territories of the hospital grouping of Loire territory (located less than 50 km away) * Whose diagnosis of episodic or chronic Cluster Headache (CH) has been confirmed according to International Classification of Headache Disorders (ICHD)- 3 criteria * With a regular sinus rhythm and heart rate

Exclusion criteria

* Conditions contraindicating the use of injectable sumatriptan * Conditions likely to affect the Autonomic Nervous System (ANS): dysautonomic sensory neuropathies, sleep apnea syndrome, etc. * Cognitive or language disorders that may interfere with pain assessment and seizure follow-up. * Patients taking treatments that may modify the Autonomic Nervous System (ANS): catecholamine (adrenaline, noradrenaline, dopamine), B-stimulants (isoprenaline, dobutamine, dopexamine, salbutamol, terbutaline, fenoterol, orciprenaline, clenbuterol, salmeterol, formoterol), B-blockers, alpha-stimulants (midodrine, alpha-methyl-dopa, clonidine, rilmenidine, moxonidine), alpha-blockers (phentolamine, prazosin, urapidil), amphetamine, tyramine, ephedrine, selegiline, cocaine, imipramine. * Impossibility to submit to the medical follow-up of the program for geographical, social or psychological reasons. * Patient deprived of liberty or under guardianship. * Patient with preventive background treatment of Cluster Headache (CH).

Design outcomes

Primary

MeasureTime frameDescription
Low Frequency/High Frequency (LF/HF) ratio at the onset of the first night seizureDay: 7Comparison of the Low Frequency/High Frequency (LF/HF) ratio at the onset of the first night seizure during the basal period, pre-seizure, seizure and after the seizure.

Secondary

MeasureTime frameDescription
Low Frequency/High Frequency (LF/HF) ratio at the onset of the first daytime seizureDay: 7Comparison of the Low Frequency/High Frequency (LF/HF) ratio at the onset of the first daytime seizure during the basal period, pre-seizure, seizure and after the seizure.
Low Frequency during daytime and night seizureDay: 7Comparison of measure of Low Frequency during daytime and night seizure.
High Frequency (HF) during daytime and night seizureDay: 7Comparison of measure of High Frequency (HF) during daytime and night seizure.
Correlation between several parametersDay: 7Correlation between Heart Rate Variability (HRV), changes in the Low Frequency/High Frequency (LF/HF) ratio, the Low Frequency (LF) and the High Frequency (HF), and the intensity of pain measured on the Visual Analog Scale (VAS).

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026