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临床试验/NCT04901767
NCT04901767已完成不适用

Comparison of Intracoronary Endothelial Dysfunction in Patients With Coronary Artery Disease Treated With Drug Coated Balloon Angioplasty and Drug Eluting Stents

Norfolk and Norwich University Hospitals NHS Foundation Trust1 个研究点 分布在 1 个国家目标入组 14 人开始时间: 2021年3月23日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
14
试验地点
1
主要终点
Fractional change in coronary artery diameter and surface area within treated segment

研究概览

简要总结

Use of intracoronary acetylcholine to investigate endothelial function in coronary arteries treated with either drug coated balloon angioplasty of drug eluting stents.

详细描述

The primary objective is to establish the differences in vasomotor response of a DCB and DES treated artery by measurement of the percentage change in coronary surface area pre and post acetylcholine administration. This will be measured with incremental doses of acetylcholine at levels both proximally and distally to the site of treatment Also is to see how far endothelial dysfunction may propagate from an interventional site by measuring drug induced dilatation/constriction as in response to acetylcholine administration. This vasomotor response will be measured in the target vessel at extended distances from the treated segment.

To achieve a meaningful comparison, 34 patients will be recruited of which 17 patients would form either arm of the study having had either a DCB or DES.

The study will be performed at the Norfolk and Norwich University Hospital and patients will be enrolled prior to a second procedure. This may occur immediately after their stent or drug coated balloon treatment or if they re-attend hospital in the following recruitment period and this may include patients for a variety of different indications.

Patients who have a scheduled, clinically indicated procedure will be eligible to be recruited as participants. They must also fulfil the inclusion criteria and not be affected by any of the exclusion criteria.

A member of the research team will provide the Patient Information Sheet to potential participants and confirm that they would be happy to be contacted subsequently to discuss the proposed research. The subsequent contact will be undertaken by a clinical research fellow, who is both a member of the Norfolk and Norwich University Hospital NHS clinical team as well as the research team, prior to their subsequent visit to discuss the study, answer any questions and confirm if they fulfil the inclusion criteria. In view of Covid-19, to reduce in hospital exposure, we might instead opt to send the patient information to the eligible patients by post, and follow with a telephone call to confirm receipt.

研究设计

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

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

  • Participant is willing and able to give informed consent for participation in the study.
  • Male or Female, aged 18 years or above.
  • Been treated with percutaneous coronary intervention of either drug coated balloon or drug eluting stent

排除标准

  • Any contraindications to administration of acetylcholine or GTN
  • History of coronary vasospasm or spontaneous coronary artery dissection
  • Significant medical, surgical or psychiatric disease that would affect subject safety or influence the study outcome according to physician's opinion
  • Patients who received a combination of drug eluting stents and drug coated balloon to the same vessel
  • Significant renal impairment (estimated glomerular filtration rate <30mL/min/ 1.73m2
  • Body mass index >35 (may affect coronary artery diameter qualitative assessment)
  • Symptomatic congestive cardiac failure
  • Severe asthma
  • Significant autoimmune inflammatory conditions (for example rheumatoid arthritis)
  • Patients taking immunomodulating drugs (including Methotrexate, Ciclosporin, steroids)
  • Previous heart transplant
  • Relative Anaemia - Haemoglobin <12g/dL in men and <10g/dL in women
  • Women of child bearing age with a positive pregnancy test

结局指标

主要结局

Fractional change in coronary artery diameter and surface area within treated segment

时间窗: 3-6 months

Will be expressed as a percentage. I.e. we will measure the diameter in mm and area in mm2 before and after.

次要结局

  • Fractional change in coronary artery diameter and surface area with increments from area of treatment(3-6 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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