Heart risk under the microscope: verapamil for cluster headaches
NCT ID NCT04406259
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study looks at how often a common heart side effect (first-degree atrioventricular block) occurs when verapamil is used at high doses to prevent cluster headaches. Researchers will monitor 60 patients starting or already on verapamil, using ECGs and blood tests. The goal is to better understand and track these heart conduction issues, not to test if verapamil works.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Verapamil
- What this could lead to
- If successful, this could help doctors better understand and manage the heart-related side effects of high-dose verapamil when used for cluster headache prevention.
- What could go wrong
- This is a small, observational study focused on side effects, not on whether verapamil works for headaches. It may not lead to new treatments or change current practice.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Phase 4
Runs after approval, following long-term safety and how well the treatment works in everyday use.
- Participants
-
About 60 people
The number the study aims to enrol. It can still change while the study runs.
- Started
-
Nov 2020
- Expected to finish
-
Sep 2027
An estimate. End dates often move.
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 years and older
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * patient 18 years old, and older * patient suffering from Cluster Headache (according to the l'ICHD-3 diagnostic criterias) * patients affiliated to the social security * patient that has given his full written consent to participate in the study * female patients participating in the study must be using an efficient contraception for more than 1 month prior to the beginning of the study Exclusion Criteria: * patient presenting contraindications to the use of verapamil * patient observing a treatment with ivabradine (Procoralan®), bétablockers, colchicine, l'esmolol, triazolam, quinidine. * patient under justicial protection * patient breastfeeding, or pregnant * patient suffering from a neuromuscular transmisson disease * patient with a pacemaker
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
AP-HP Hôpital la Timone
Marseille, 13005, France
-
CHU de Nice
Nice, CHUN, 06003, France
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Other studies related to the condition(s) this trial covers.
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