Trials / Completed
CompletedNCT04218760
Multiomics After Headache Provocation of People Who Are Unable to Have Headache
Pain Perception, Headache Provocation and Multiomics of People Who Are Unable to Have Headache
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 58 (actual)
- Sponsor
- Danish Headache Center · Academic / Other
- Sex
- Male
- Age
- 18 Years – 70 Years
- Healthy volunteers
- Not accepted
Summary
Headaches are extremely common illnesses with a combined lifetime prevalence of 90-99% in Europe. Despite this high prevalence, there are persons who have never, in their whole life, encountered a headache. The aim of the study is to identify factors that protect against headache by studying multiomics in people who never have had a headache (headache resistant) versus non-resistant controls. The investigators will measure multiomic changes (transcriptomics and metabolomics) after headache provocation with isosorbide mononitrate. 3 blood samples, two for RNA and one for metabolomics are taken right before administration of isosorbide mononitrate, 3 hours after administration of isosorbide mononitrate and again 5 hours after administration of isosorbide mononitrate. The investigators hope to contribute with novelty to the current understanding of headache pathophysiology and development of more efficient treatment of headache.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Isosorbide Mononitrate 60 MG Extended Release Oral Tablet [Imdur] | 1 tablet Isosorbide Mononitrate 60 mg administrated orally. |
| OTHER | Blood sample | 3 blood samples from a periferal vein, two for RNA and one for metabolomics are taken right before administration of isosorbide mononitrate, 3 hours after administration of isosorbide mononitrate and again 5 hours after administration of isosorbide mononitrate. |
Timeline
- Start date
- 2019-10-10
- Primary completion
- 2020-03-12
- Completion
- 2020-03-12
- First posted
- 2020-01-06
- Last updated
- 2021-03-25
Locations
1 site across 1 country: Denmark
Source: ClinicalTrials.gov record NCT04218760. Inclusion in this directory is not an endorsement.