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Sumatriptan non-responders: evaluation of a possible biomarker.

Sumatriptan non-responders: evaluation of a possible biomarker.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON27172
Enrollment
21
Registered
2013-09-10
Start date
2013-09-10
Completion date
Unknown
Last updated
2024-02-28

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

Conditions

Migraine

Interventions

S.C. injection of sumatriptan

Sponsors

Erasmus MC
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: • Age between 18 and 50 years • Male or female • Females should use an oral contraceptive pill • Non-smoking for > 6 months • Body mass index between 18 and 30 kg/m^2 • Capable and willing to give informed consent • General good health, based on medical history and physical examination

Exclusion criteria

Exclusion criteria: • History of cardiovascular disease • Perimenopausal status of females • Any serious illness that can compromise study participation • Use of any medication (e.g., NSAIDs, other analgesics) < 48 hrs before the study • Dermal diseases at the upper frontal side of the face • Pregnancy or breastfeeding • History of sensitivity to the fruits of capsicum plants (e.g. chilli peppers) • Alcohol or drug abuse

Design outcomes

Primary

MeasureTime frame
Percentage of change in dermal blood flow response to capsaicin application and saline iontophoresis after sumatriptan or placebo administration.

Secondary

MeasureTime frame
• Heat sensation after capsaicin application • Blood pressure changes after sumatriptan use

Contacts

Public ContactA.H. Meiracker, van den

Erasmus MC

a.vandenmeiracker@erasmusmc.nl+31-10-4639222

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)