Comparison of two doses of norepinephrine infusion for prophylaxis of maternal hypotension following spinal anaesthesia in pregnant women undergoing emergency c-section: a two arm, double blind randomised control trial - NI

All India Institute of Medical Sciences, Bihar0 个研究点目标入组 0 人开始时间: 待定最近更新: 2024年6月24日

研究概览

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•Labouring and non-labouring pregnant women with period of gestation more than 37 weeks undergoing category II caesarean section.
•Non-reassuring cardiotocography (CTG) including anyone of the following-
•Fetal heart rate(FHR) as per RCOG guidelines (FHR 100-109bpm or 161-180bpm).
•Variability less than 5bpm for more than 40minutes but less than 90 minutes.
•Early deceleration.
•Variable deceleration.
•Single prolonged deceleration less than 90 seconds

•Complications such as hypertensive disorders of pregnancy, cardiovascular or cerebrovascular disease, multiple gestation, known fetal abnormality.
•Hemodynamically unstable or baseline SBP less than 100 mmHg.
•ASA physical status 3 or more than 3.
•Severely compromised fetus who requires immediate administration of general anaesthesia.
•Presence of contra-indications for spinal anaesthesia.
•Participants who have received labour analgesia.

发起方

All India Institute of Medical Sciences, Bihar