跳至主要内容
临床试验/NCT05854992
NCT05854992已完成不适用

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

Mayo Clinic3 个研究点 分布在 1 个国家目标入组 68,419 人开始时间: 2022年7月5日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
发起方
Mayo Clinic
入组人数
68,419
试验地点
3
主要终点
Major adverse cardiovascular events (MACE)

研究概览

简要总结

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

详细描述

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.

研究设计

研究类型
Observational
观察模型
Other
时间视角
Retrospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

Cardiovascular Risk Group Treated with Triptans

Subjects with diagnosis of migraine and cardiovascular disease, cerebrovascular disease and/or two or more cardiovascular risk factors who received Triptans as part of clinical care.

干预措施: Acute migraine treatment with any prescribed triptans (Drug)

Cardiovascular Risk Control Group Treated with No Triptans

Subjects with who did not received Triptans as part of clinical care.

干预措施: Standard of care management of acute migraine without triptans (Drug)

Pregnant Women Group Treated with Triptans

Subjects diagnosed with migraine that received Triptans as part of clinical care during pregnancy.

干预措施: Acute migraine treatment with any prescribed triptans (Drug)

Pregnant Women Control Group Treated with No Triptans

Subjects that did not receive Triptans as part of clinical care during pregnancy.

干预措施: Standard of care management of acute migraine without triptans (Drug)

结局指标

主要结局

Major adverse cardiovascular events (MACE)

时间窗: 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

Full term birth

时间窗: 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

次要结局

  • Heart failure(60 days of starting treatment)
  • Revascularization(60 days of starting treatment)
  • Pre-term delivery(37 0/7 weeks of gestation through 38 6/7 weeks of gestation)
  • all-cause death(60 days of starting treatment)
  • Nonfatal stroke(60 days of starting treatment)
  • Nonfatal myocardial infarction(60 days of starting treatment)
  • Transient cerebral ischemia(60 days of starting treatment)
  • Tubal or ectopic pregnancy(up to delivery)
  • Cesarean section delivery(up to delivery)
  • Spontaneous abortions/miscarriage(up to delivery)
  • Fetal death/stillbirth(up to delivery)
  • Intra-uterine growth restriction(up to delivery)
  • Eclampsia/preeclampsia(up to delivery)
  • Major fetal malformations(up to delivery)

研究者

发起方
Mayo Clinic
申办方类型
Other
责任方
Principal Investigator
主要研究者

M. Hassan Murad, M.D.

Principal Investigator

Mayo Clinic

研究点 (3)

Loading locations...

相似试验