跳至主要内容
临床试验/CTRI/2024/04/066396
CTRI/2024/04/066396尚未招募不适用

A Descriptive study of Adverse Drug Reactions with Causality Assessment and Potential Drug Interactions in the Outpatients of the Psychiatric Department at SMS Hospital Jaipur.

Dr. Kapil Goyal1 个研究点 分布在 1 个国家目标入组 600 人开始时间: 2024年5月6日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
600
试验地点
1
主要终点
1. To report and evaluate patterns of Adverse Drug Reactions (ADRs) occurring due

研究概览

简要总结

Under-reporting is a problem with ADRs occurring due to psychotropic drugs. The need for this study is for observation and analysis of the ADRs occurring due to psychotropic drugs and then assessing all the reported ADRs for Causality using World Health Organization-Uppsala Monitoring Centre (WHO-UMC) scale. Also, studying the potential drug-drug interactions (pDDIs) amongst different psychotropic drugs as well as between psychotropic drugs and other co-prescribed drugs by using Medscape software (online) (http://reference.medscape.com/drug-interactionchecker) will aid clinicians to achieve optimal therapeutic outcomes in patients by increasing awareness of clinically relevant psychotropic drug interactions. It will also help to sensitize the healthcare workers as well as the patients and their attendant for reporting of ADRs occurring due to psychotropic medications.

研究设计

研究类型
Observational

入排标准

年龄范围
18.00 Year(s) 至 60.00 Year(s)(—)
性别
All

入选标准

  • Patients attending the Psychiatric OPD for follow up, who were diagnosed to be suffering from any psychiatric illness and prescribed at least one psychotropic drug.
  • Patients of either sex.
  • Patients in the age group of 18 years to 60 years.
  • Patients who will give informed consent.

排除标准

  • Patients having mental and behavioural disorders due to psychoactive substance use.
  • Patients who are pregnant/ lactating women.
  • Patients who are part of any other study.
  • Patients who will be non-co-operative.

结局指标

主要结局

1. To report and evaluate patterns of Adverse Drug Reactions (ADRs) occurring due

时间窗: 6 Months

to psychotropic drugs.

时间窗: 6 Months

2. To assess all the reported ADRs for Causality using WHO-UMC scale.

时间窗: 6 Months

3. To study the potential drug-drug interactions (pDDIs) among different

时间窗: 6 Months

psychotropic drugs as well as between psychotropic drugs and other co-prescribed

时间窗: 6 Months

drugs by using Medscape software (online) (http://reference.medscape.com/druginteractionchecker).

时间窗: 6 Months

次要结局

  • 1. To process the reported ADRs to Indian Pharmacopoeia Commission (IPC)(Ghaziabad by using VIGIFLOW software.)

研究者

发起方
Dr. Kapil Goyal
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

Dr Kapil Goyal

SMS Medical College

研究点 (1)

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