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Completed

NCT Number: NCT05854992

Treatments of Migraine with Triptans in Individuals with Elevated Cardiovascular Risk and in Pregnant Women

Researchers are evaluating the safety of triptan treatment of migraine in individuals with elevated cardiovascular risk and in pregnant women.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Mayo Clinic Arizona, Phoenix, Arizona, United States

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About this study

Migraine is a very common condition that can be associated with significant morbidity. For the acute treatment of migraine attacks, the use of triptans, NSAIDs, acetaminophen, dihydroergotamine, calcitonin gene-related peptide antagonists, lasmiditan, and some nonpharmacologic treatments are associated with improved pain and function. The effectiveness of these therapies has been documented in various studies and summarized in systematic reviews. However, systematic reviews have demonstrated evidence gaps in two groups of patients that were excluded from treatment trials. These are patients with cardiovascular disease or at high risk of cardiovascular events, and pregnant women.

Triptans, the mainstay treatment for migraine attacks and the one supported by the highest quality evidence, are considered vasoactive and are contraindicated per formulary in individuals who have a history of myocardial infarction, stroke, or uncontrolled vascular risk factors such as hypertension. These individuals are usually excluded from randomized trials. Similarly, pregnant women have been excluded from triptans trials and the observational studies offered low certainty evidence about their safety. Yet, 44% of surveyed members of the American Headache Society reported being somewhat or very comfortable using triptans in pregnancy.

Therefore, the investigators intend to evaluate the safety of triptan treatment of migraine in individuals with cardiovascular disease or multiple cardiovascular risk factors, and in pregnant women in two target trial emulations.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Treatments of Migraine With Triptans in Individuals With Elevated Cardiovascular Risk:

Inclusion:

  • Aged >=18 years
  • At least 1 year history of migraine with or without aura
  • Confirmed cardiovascular or cerebrovascular disease, including myocardial infarction (MI), coronary artery disease (CAD), cerebrovascular disease, stroke; or at least 2 cardiovascular risk factors, including diabetes, hyperlipidemia, hypertension, obstructive sleep apnea, peripheral vascular disease;
  • At least 1 year of prior triptan treatment or no previous triptan treatment.

Exclusion:

  • Prescription of ergot alkaloids or dihydroergotamine within 60 days before or after starting treatment

Treatments of Migraine With Triptans in Pregnant Women

Inclusion:

  • Aged >=18 years
  • Pregnant woman
  • Diagnosis of episodic or chronic migraine with or without aura before pregnancy

Exclusion:

  • Prescription of ergot alkaloids or dihydroergotamine <= 60 days before pregnancy or during pregnancy

Treatment and study plan

Acute migraine treatment with any prescribed triptans

Drug

Sumatriptan, treximet (sumatriptan/naproxen combination), zolmitriptan, naratriptan, rizatriptan, almotriptan, eletriptan, and frovatriptan. No restriction on dose, frequency, duration, or delivery routes.

Other names: Triptans

Standard of care management of acute migraine without triptans

Drug

Any standard of care management without triptans

Other names: No triptans

Primary outcomes

  1. Major adverse cardiovascular events (MACE)

    Time frame: 60 days of starting treatment

    Treatments of Migraine With Triptans in Individuals With Elevated Cardiovascular Risk: number of subjects to experience major adverse cardiovascular events (MACE) which consists of all-cause death, nonfatal myocardial infarction, nonfatal stroke, heart failure, transient cerebral ischemia, or revascularization

  2. Full term birth

    Time frame: 39 0/7 weeks of gestation through 40 6/7 weeks of gestation

    Treatments of Migraine With Triptans in Pregnant Women: number of pregnant women to have a full term birth

Secondary outcomes

  1. all-cause death

    Time frame: 60 days of starting treatment

    Treatments of Migraine With Triptans in Individuals With Elevated Cardiovascular Risk: all-cause death

  2. Nonfatal myocardial infarction

    Time frame: 60 days of starting treatment

    Treatments of Migraine With Triptans in Individuals With Elevated Cardiovascular Risk: nonfatal myocardial infarction

  3. Nonfatal stroke

    Time frame: 60 days of starting treatment

    Treatments of Migraine With Triptans in Individuals With Elevated Cardiovascular Risk: nonfatal stroke

  4. Heart failure

    Time frame: 60 days of starting treatment

    Treatments of Migraine With Triptans in Individuals With Elevated Cardiovascular Risk: Heart failure

  5. Transient cerebral ischemia

    Time frame: 60 days of starting treatment

    Treatments of Migraine With Triptans in Individuals With Elevated Cardiovascular Risk: transient cerebral ischemia

  6. Revascularization

    Time frame: 60 days of starting treatment

    Treatments of Migraine With Triptans in Individuals With Elevated Cardiovascular Risk: revascularization

  7. Pre-term delivery

    Time frame: 37 0/7 weeks of gestation through 38 6/7 weeks of gestation

    Treatments of Migraine With Triptans in Pregnant Women: Pre-term delivery

  8. Cesarean section delivery

    Time frame: up to delivery

    Treatments of Migraine With Triptans in Pregnant Women: cesarean section delivery

  9. Spontaneous abortions/miscarriage

    Time frame: up to delivery

    Treatments of Migraine With Triptans in Pregnant Women: Spontaneous abortions/miscarriage

  10. Fetal death/stillbirth

    Time frame: up to delivery

    Treatments of Migraine With Triptans in Pregnant Women: Fetal death/stillbirth

  11. Intra-uterine growth restriction

    Time frame: up to delivery

    Treatments of Migraine With Triptans in Pregnant Women: Intra-uterine growth restriction

  12. Eclampsia/preeclampsia

    Time frame: up to delivery

    Treatments of Migraine With Triptans in Pregnant Women: Eclampsia/preeclampsia

  13. Tubal or ectopic pregnancy

    Time frame: up to delivery

    Treatments of Migraine With Triptans in Pregnant Women: Tubal or ectopic pregnancy

  14. Major fetal malformations

    Time frame: up to delivery

    Treatments of Migraine With Triptans in Pregnant Women: Major fetal malformations

Sponsors and collaborators

Lead sponsor

Mayo Clinic

Other

Collaborators

  • Agency for Healthcare Research and Quality (AHRQ)

Registry information

Important dates

Study start
2022
Primary completion
2024
Study completion
2024
First posted
May 11, 2023
Registry last updated
Dec 2, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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