跳至主要内容
临床试验/CTRI/2023/08/056622
CTRI/2023/08/056622尚未招募3 期

A study to evaluate fetomaternal outcome with varying doses of hyperbaric levobupivacaine and fentanyl as an adjuvant in cesarean section under spinal anaesthesia - nil

Sri Guru Ram Das Institute of Medical Sciences and Research0 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
3 期
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
Interventional

入排标准

入选标准

  • 1. Patients undergoing elective LSCS.
  • 2. Patients American Society of Anaesthesiology(ASA) Grade II.
  • 3. Patients having height >150cm
  • 4. Patients having period of gestation equal to or above 35 weeks, with a live singleton foetus.

排除标准

  • 1. Patient given refusal for study
  • 2. Patient with absolute contraindication for subarachnoid block (spinal
  • deformity, local sepsis).
  • 3. Patient with Cardiorespiratory problems.
  • 4. Patient with Coagulation disorder.
  • 5. Patient with Neurological disease
  • 6. Patient with Psychological disease
  • 7. Patient with Endocrine disease and allergy to used drugs

研究者

发起方
Sri Guru Ram Das Institute of Medical Sciences and Research

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