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临床试验/CTRI/2022/01/039569
CTRI/2022/01/039569尚未招募未知

Development of optimal management strategy in acute Paraquat poisoning: a toxicokinetic approach

Dr TMA Pai Fellowship0 个研究点目标入组 0 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
尚未招募
发起方

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

入选标准

  • Objective 1 and 2:
  • Patients who arrive at the Emergency ward with paraquat poisoning (confirmed by a qualitative test) within 24 hours of exposure. Patients will be included above 18 years of age, irrespective of gender, time from exposure, route of exposure (oral, inhalational or direct contact) and type of exposure (suicidal or accidental).
  • Objective 3:
  • Patients enrolled in Objective 1 and 2 and expired during hospital stay who are sent for routine post-mortem examination.

排除标准

  • Objective 1 and 2:
  • Pregnant or lactating patients; patients with critical illness(es) such as cancer, patients having history of organ transplantation, patients who are already on immunosuppressants for specific medical conditions, patients exposed to paraquat with other toxic agents, patients referred from primary care and other facilities (after 24 hours of exposure), patients with incomplete data, patients lost to follow-up and patients/relatives/guardians who refuse to consent.
  • Objective 3:
  • Relatives/guardian who refuse consent.

研究者

发起方
Dr TMA Pai Fellowship

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