跳至主要内容
临床试验/CTRI/2025/08/092807
CTRI/2025/08/092807尚未招募Unknown

Cardiac Rhythm and Heart Failure Product Surveillance Registry (PSR) Platform Base - Triage HF India

India Medtronic Pvt Ltd11 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2025年9月10日最近更新:

试验速览

阶段
Unknown
状态
尚未招募
入组人数
100
试验地点
11
主要终点
1. All data collected from regional cohorts will contribute to the overall primary objective of safety and effectiveness of the product

研究概览

简要总结

This is a non-randomized, prospective and non-regulated study on commercial released TraigeHF which is enabled with Cobalt/Crome device. The main objective of study is to collect data from regional cohorts and assess the overall primary objective of safety and effectiveness of the commercialized product.

Study will be conducted in 10-12 sites in India with a target to enroll 100 patients. Study duration will be 2-3 years which include 12 months follow up.

Data will be collected at Baseline (consenting, eligibility, pre-procedure and Medical history), CVG procedure (Procedure type and implant) and follow-up visits.

研究设计

研究类型
Observational

入排标准

年龄范围
18.00 Year(s) 至 99.00 Year(s)(—)
性别
All

入选标准

  • Patient or legally authorized representative (LAR) provides authorization and/or consent per institution and geographical requirements
  • Patient has, or is intended to receive or be treated with, an eligible Medtronic product
  • Patient is consented within the enrollment window of the therapy received, as applicable
  • Additional Therapy-specific components if needed.

排除标准

  • Patient who is, or is expected to be, inaccessible for follow-up
  • Participation is excluded by local law
  • Patient is currently enrolled or plans to enroll in concurrent drug/device study that may confound the PSR results
  • Additional Therapy-specific components if needed.

结局指标

主要结局

1. All data collected from regional cohorts will contribute to the overall primary objective of safety and effectiveness of the product

时间窗: Baseline, Implant/ Procedure, 12 months follow up

2. The primary effectiveness objective is to estimate the positive predictive value (PPV) of HFRS high risk status associated with worsening heart failure.

时间窗: Baseline, Implant/ Procedure, 12 months follow up

次要结局

  • 1. Summarize the number of subsequent heart failure hospitalization (HFH) or HF related deaths that were not preceded by a high Heart Failure Risk Status.(2. Compare the incidence in subsequent heart failure hospitalization between subjects with actions taken based on HFRS and subjects without actions taken.)

研究者

申办方类型
Other [Medical Device Industry]
责任方
Principal Investigator
主要研究者

Vinay Rajan

India Medtronic Pvt Ltd

研究点 (11)

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TriageHF India Study | 临床试验