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临床试验/PACTR202402621085427
PACTR202402621085427尚未招募Unknown

A Comparative Evaluation Of Propofol Versus Dexmedetomidine Effects On Haemodynamic Responses, Seizure Duration And Recovery Profile Following Electroconvulsive Therapy

SELF FUNDED0 个研究点目标入组 76 人开始时间: 2024年2月4日最近更新:
适应症

试验速览

阶段
Unknown
状态
尚未招募
发起方
入组人数
76

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
19 Year(s) 至 44 Year(s)(—)
性别
All

入选标准

  • 1.Age 18 years and above.
  • 2.Patients with American Society of Anesthesiologists (ASA) physical status class I or II.

排除标准

  • 1.Refusal of Patient or guardian to give written informed consent.
  • 2.Age below 18 years.
  • 3.Patient with ASA > II
  • 4.History of allergy or sensitivity to the study medications.
  • 5.Presence or evidence of raised intracranial pressure.
  • 6.Presence of glaucoma
  • 7.Present or recent myocardial infarction (by history or ECG, lab results).
  • 8.Anticipated difficult airway
  • 9.Systemic hypertension

研究者

发起方
SELF FUNDED

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