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临床试验/NCT06696807
NCT06696807已完成不适用

The Effects of Immunomodulatory Therapy in Patients with Vasospastic Angina

Dao Wen Wang1 个研究点 分布在 1 个国家目标入组 71 人开始时间: 2018年10月1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
入组人数
71
试验地点
1
主要终点
adverse outcomes

研究概览

简要总结

Vasospastic angina (VSA) is caused by brief spasms of the main coronary artery and its major branches, resulting in varying degrees of luminal occlusion. Although vasodilator therapy is widely used and significantly alleviates VSA symptoms, it has not led to notable improvements in the prognosis of patients with VSA. Recent studies have suggested that inflammation plays a crucial role in VSA. This study aimed to evaluate the potential effectiveness of immunomodulatory therapy for improving patient prognosis.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

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

入选标准

  • (1) Transient total or subtotal occlusion of the coronary artery (contraction >90%) observed either spontaneously or in response to irritant stimulation (typically acetylcholine, ergot, or hyperventilation); (2) Presence or absence of ischemic electrocardiogram changes during episodes; (3) Nitrate-responsive angina during spontaneous episode: rest angina and/or marked diurnal variation in exercise tolerance and/or episodes precipitated by hyperventilation and/or suppression of episodes by calcium channel blockers.

排除标准

  • (1) age 15 years or older; and (2) suspected VSA with chest pain and evidence of coronary spasm, or VSA diagnosed intraoperatively or at discharge.
  • The following exclusion criteria were applied: (1) failure to meet the diagnostic criteria for VSA; (2) presence of aortic disease, cardiomyopathy, malignant tumor, Kounis syndrome, or other diseases that may affect the outcome; (3) insufficient clinical data available; and (4) loss to follow-up.

研究组 & 干预措施

immunomodulatory therapy group

who received glucocorticosteroids and/or IVIG in addition to traditional therapy.

干预措施: glucocorticosteroids and/or intravenous immunoglobulin (Drug)

结局指标

主要结局

adverse outcomes

时间窗: From Feb 2017 to Feb 2024

readmissions due to the onset of coronary spasm or VSA, MACE (including non-fatal stroke, non-fatal myocardial infarction, cardiovascular death) and all-cause death

次要结局

未报告次要终点

研究者

发起方
Dao Wen Wang
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Dao Wen Wang

Professor

Tongji Hospital

研究点 (1)

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