| Registry | NCT03609008 |
|---|---|
| Status | Completed |
| Phase | Not applicable |
| Study type | Interventional; randomized, parallel, masking: quadruple, other |
| Enrollment | 20 (Actual) |
| Sponsor | Danish Headache Center (Other) |
| Conditions | Dilatation of Cranial Arteries; MMA, STA and MCA, Headache |
| Interventions | Levcromakalim, Saline (Drug) |
| Dates | start 2018-06-26, primary completion 2018-08-15, completion 2018-08-15, first posted 2018-08-01, last updated 2022-07-05 |
| Locations | 1 site in Denmark |
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All trials for Dilatation of Cranial Arteries; MMA, STA and MCA All trials for Headache All trials of Levcromakalim All trials of Saline
Healthy participants vill randomly be allocated in a 2:1 order to receive 1 mg levcromakalim or placebo (isotonic saline) for 20 min.
The investigator here examine the effect of levcromakalim infusion on the MMA and the MCA circumference over several hours using a high resolution MRA technique in a randomized, double-blind placebo-controlled design in healthy volunteers. The investigator hypothesized that levcromakalim induces dilatation of cranial arteries.
Healthy participants vill randomly be allocated in a 2:1 order to receive 1 mg levcromakalim or placebo (isotonic saline) for 20 min.
The investigator here examine the effect of levcromakalim infusion on the MMA and the MCA circumference over several hours using a high resolution MRA technique in a randomized, double-blind placebo-controlled design in healthy volunteers. The investigator hypothesized that levcromakalim induces dilatation of cranial arteries.
MR imaging will be performed on a 3.0 Tesla Philips Achieva Scanner (Philips Medical Systems, Best, The Netherlands) using an eight-element phased-array receiver head coil. We will obtain repeated MRA measurements covering the MMA and MCA before and after levcromakalim/placebo infusion
| Arm | Type | Interventions | Description |
|---|---|---|---|
| Levcromakalim | Active comparator | Drug: Levcromakalim | 18 participants will randomly be allocated in a 2:1 order to receive 1 mg levcromakalim or placebo (isotonic saline) |
| Saline | Placebo comparator | Drug: Saline | 18 participants will randomly be allocated in a 2:1 order to receive 1 mg levcromakalim or placebo (isotonic saline) |
Sex: All, ages: 18 Years to 60 Years, accepts healthy volunteers
Inclusion Criteria: * Healthy volunteers of both sexes. * 18-60 years. * 50-100 kg. * Women of childbearing potential must use adequate contraception. Exclusion Criteria: * A history of serious somatic disease * Migraine or any other type of headache (except episodic tension-type headache less than once a month) * Daily intake of any medication except contraceptives * Contraindications for MRI scan.
| Facility | City | Country | Status |
|---|---|---|---|
| Danish headache center | Copenhagen, Glostrup | Denmark |