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临床试验/CTRI/2025/02/080723
CTRI/2025/02/080723尚未招募不适用

Standardization, scientific validation and automation of Taila Bindu Pariksha- an ancient prognostic tool

Director General, CCRAS1 个研究点 分布在 1 个国家目标入组 225 人开始时间: 2025年3月3日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
225
试验地点
1
主要终点
Fabrication of an automated device to

研究概览

简要总结

An automated device will be fabricated to minimize the manual errors. After fabrication of the  automated device, a total of 225 human healthy volunteers will be selected after confirming their normal health condition and their urine will be subjected to Taila Bindu Pariksha. The data will be recorded and will be analyzed for establishing normal reference value for Taila Bindu Pariksha in healthy people

研究设计

研究类型
Observational

入排标准

年龄范围
18.00 Year(s) 至 25.00 Year(s)(—)
性别
All

入选标准

  • •Participants having normal urine parameters and normal LFT and RFT
  • •Participants having no severe diseases and no medication in last seven days
  • •Participants who will be able to give written informed consent.

排除标准

  • •Participants having abnormal LFT and RFT and abnormality in urine examination
  • •Participants enrolled in any other study
  • •Participant to whom the investigator thinks will jeopardize the study.

结局指标

主要结局

Fabrication of an automated device to

时间窗: At Baseline

minimize the variations in standardized

时间窗: At Baseline

parameters

时间窗: At Baseline

次要结局

  • 1. Establishment of the reference value of Taila Bindu Pariksha in healthy individuals

研究者

发起方
Director General, CCRAS
申办方类型
Research institution
责任方
Principal Investigator
主要研究者

Anukul Chandra Kar

Faculty of Ayurveda, Institute of Medical Sciences, Banaras Hindu University

研究点 (1)

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