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临床试验/CTRI/2019/02/017466
CTRI/2019/02/017466尚未招募4 期

Efficacy of the Valsalva manoeuvre on propofolinjection pain: A randomized controlled study

Indira Gandhi Institute of Medical Sciences0 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
4 期
状态
尚未招募

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

入选标准

  • 1.Patients of ASA physical status 1 and 2
  • 2.Patients between 18 â?? 60 years of age of either sex
  • 3.Patients able to comprehend and willing to participate.
  • 4.Patients who are able to hold the sphygmomanometer up to 40 mm Hg for a period of at least 15 s
  • 5.Patients in whom propofol is indicated for induction of anaesthesia.

排除标准

  • 1.Patientâ??s refusal to participate
  • 2.Patients with known sensitivity to lignocaine or propofol
  • 3.Patients on concomitant analgesic or sedative medication
  • 4.Patients with presence of infection on the dorsum of the left hand
  • 5.Patients in whom Valsalva manoeuvre is contraindicated (e.g. raised intracranial or intraocular pressure, glaucoma, retinopathy, middle ear pathology etc)
  • 6.Patients who are unable to hold the sphygmomanometer up to 40 mm Hg for a period of at least 15 s

研究者

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