跳至主要内容
临床试验/CTRI/2021/05/033379
CTRI/2021/05/033379Other未知

A double blinded prospective randomised control study of pre-operative administration of intravenous Mephentermine vs intramuscular Mephentermine in preventing post spinal hypotension in Caesarean section

Office of the Principal Midnapore Medical College and Hospital0 个研究点目标入组 67 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
Other
发起方
入组人数
67

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

  • All pregnant mothers posted for lower
  • segment caesarean section under spinal anaesthesia and can give informed consent for
  • participation.

排除标准

  • i. Less than 18 years of age
  • ii. ASA grade III & above
  • iii. More than 35 years of age
  • iv. Having 2 lower segment caesarean section previously
  • v. Having systolic blood pressure more than 140 mm Hg or diastolic blood pressure more
  • than 90 mm Hg pre operatively
  • vi. On anti-hypertensive medication(s)
  • vii. Patients having gestational diabetes mellitus
  • viii. Having Twin or multifetal pregnancy
  • ix. Refusing to give consent
  • x. Any cases where repeat spinal administration will be needed (Failed Spinal).
  • xi. Any cases which may be needed to be converted in to general anaesthesia
  • xii. Contraindication to spinal anaesthesia
  • xiii. Patients having severe pallor
  • xiv. Any operation lasting for more than 90 minutes
  • xv. Foetal malformation or malpresentation
  • xvi. Drug allergy to study drugs
  • xvii. Any cases which require other rescue vasopressors during the procedure
  • xviii. Emergency cases like
  • 1. Foetal bradycardia
  • 2. Impending rupture
  • 3. heart disease
  • 4. ante partum haemorrhage
  • 5. Cord prolapses

研究者

发起方
Office of the Principal Midnapore Medical College and Hospital

相似试验