跳至主要内容
临床试验/NCT02136706
NCT02136706撤回不适用

Feasibility and Diagnostic Accuracy of Myocardial SPECT Using Early Imaging Protocol: A Pilot Study

Medhat Osman MD0 个研究点开始时间: 2015年12月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
撤回
发起方
主要终点
Visual and semi-quantitative evaluation of W10 and W30 studies.

研究概览

简要总结

Encouraged by the recent data published ,the investigators think that a waiting time of 10 minutes is feasible while preserving diagnostic accuracy and would like to assess the feasibility and diagnostic efficacy of W10 compared with W30 imaging in a pilot study. By combining W10 imaging with half-time acquisition, the time of the technetium-99m myocardial perfusion imaging procedure could be shortened by at least 50%, lasting only 40 minutes for W10 (10-minute waiting) imaging compared with 90 minutes for W30 imaging (30-minute waiting).

The investigators hypothesize that (1) W10 MPI is clinically feasible and tolerable by the patients, that (2) W10 MPI provides high image quality and that (3) W10 MPI provides diagnostic accuracy comparable to W30 MPI.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Diagnostic
盲法
None

入排标准

年龄范围
18 Years 至 88 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Men and women ≥18 and ≤ 89 years of age of any race /ethnicity
  • •Patient has undergone or is being scheduled for a clinically indicated CardiacCath with or without angioplasty
  • •Patient may have suffered myocardial infarction more than 3 days before T99m-MPI
  • •Patient may have undergone percutaneous transluminal coronary angioplasty (PTCA) or coronary stent placement more than 3 days prior to T99m-Myocardial Perfusion Imaging (MPI)
  • •Interval between T99m-MPI and CardiacCath is within 30 days
  • •Females cannot be pregnant or lactating
  • •Women of no child-bearing potential (post-menopausal defined as amenorrhea ≥ 12 consecutive months, or because they have undergone successful surgical sterilization and deny current history of pregnancy and nursing). These subjects do not require serum pregnancy test on the day of the study
  • •Women of childbearing potential will require a negative serum pregnancy test, performed on the day of the study
  • •Provide signed Informed Consent prior to undergoing the study procedures

排除标准

  • •Patients less than 18 and ≥89 years of age
  • •Patient has been involved in any other investigative, radioactive research procedure within 7 days and during the study participation period
  • •History of 2nd or 3rd degree Atrio-ventricular-block, or sinus node dysfunction unless the patients have a functioning artificial pacemaker
  • •Current ventricular tachycardia, atrial fibrillation, atrial tachycardia, or atrial flutter
  • •Current unstable angina or cardiovascular instability
  • •Current history of exacerbated Chronic Obstructive Pulmonary Disease (COPD) or asthma
  • •Known hypersensitivity or contraindication to regadenoson or aminophylline
  • •Use of caffeinated substance, dipyridamole-containing medication, aminophylline, or xanthines containing medication (e.g. theophylline) within the 12 hours prior to Lexiscan administration

研究组 & 干预措施

10/30 min rest/stress

No Intervention

Rest and stress T99m-MPI obtained 10 minutes and 30 minutes after tracer injection. After the myocardial perfusion imaging the investigators will have 10 minute waiting period to take images and then wait the 30 minutes, standard of care to take the images.

干预措施: Myocardial Perfusion imaging with 10 minute waiting period (Procedure)

结局指标

主要结局

Visual and semi-quantitative evaluation of W10 and W30 studies.

时间窗: Day 1of testing

The investigators will evaluate image quality of W10 and W30-qualitatively (visually) by 2 independent readers and semi-qualitatively by means of region of interest (ROI) count/pixels parameters of W10 and W30 data and compare their diagnostic accuracy for the diagnosis of myocardial ischemia and infarction.

次要结局

  • Tolerability Questionnaire(Day 1 of testing)
  • Feasibility of W10 by written documentation.(Day 1 of testing)

研究者

发起方
Medhat Osman MD
申办方类型
Fed
责任方
Sponsor Investigator
主要研究者

Medhat Osman MD

Professor of Radiology, Director of Nuclear Medicine and Pet/CT

VA St. Louis Health Care System

相似试验