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临床试验/PACTR202403873496250
PACTR202403873496250已完成Unknown

Effects of Oral Clonidine Pre-medication on Intra-Operative Blood Loss during Caesarean Section under Sub-Arachnoid Block in Federal Teaching Hospital Abakaliki

Self0 个研究点目标入组 160 人开始时间: 2024年2月8日最近更新:
适应症

试验速览

阶段
Unknown
状态
已完成
发起方
Self
入组人数
160

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
Female

入选标准

  • Normotensive and mild to moderate hypertensive (controlled) pregnant women aged 18 to 45 years who were scheduled for elective caesarean section under SAB at the study centre
  • Those who consented to participate in the study.

排除标准

  • ?Patients below age 18 and above age 45years.
  • ?Grandmultiparous women (parity greater or equal to 5).
  • ?Patients with complications of pregnancy such as: placenta praevia, Abruptio placentae, pre-eclampsia with BP = 160/110mmHg, Eclampsia, pregnancy-induced hypertension or chronic hypertension in pregnancy with BP = 160/110mmHg.
  • ?Emergency Caesarean sections
  • ?Patients with Cardiovascular /Respiratory diseases
  • ?Renal/hepatic disease patients
  • ?Multiple gestations.
  • ?Patients that took antihypertensive <24 hours before surgery.
  • ?History of allergy to the study drug.
  • ?Patients with height less or equal to 1.0m.
  • ?Patients with previous caesarean section(s).

研究者

发起方
Self

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