跳至主要内容
临床试验/CTRI/2024/07/070174
CTRI/2024/07/070174尚未招募3 期

Comparative study of pre-loading and co-loading with crystalloids on the incidence of hypotension after spinal anaesthesia in cesarean delivery

BJMedical College and Civil Hospital Ahmedabad Government of Gujarat1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2024年7月16日最近更新:

试验速览

阶段
3 期
状态
尚未招募
发起方
入组人数
100
试验地点
1
主要终点
parameters compared will be SBP,DBP,MAP,PR,RR and SPO2

研究概览

简要总结

Hypotension after spinal anaesthesia is a complication that occurs in general population and in patients undergoing cesarean section .this hypotension is mainly due to sympathetic blockade which causes peripheral vasodilation and venous pooling. The risk of hypotension increases in pregnant women undergoing cesarean section that requires block levels as high as 4th thoracic segment dermatome. In addition, the risk of hypotension is also increased due to anatomic and physiological changes in pregnant women with aortocaval compression. Hypotension can cause adverse effects on both mother and foetus. Several techniques and methodologies have been adopted for the prevention of this neuraxial hypotension with varying degree of success. The administration of intravenous fluids to optimize the blood volume during sympathectomy has been the most popular and widely used as the first line of therapy. The intravenous fluids can be used both before and during the administration of spinal anaesthesia, the techniques appropriately named as pre-loading and co-loading respectively.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Participant Blinded

入排标准

年龄范围
18.00 Year(s) 至 40.00 Year(s)(—)
性别
Female

入选标准

  • parturients of ASA grade I/II posted for elective cesarean delivery giving consent for study.

排除标准

  • Patient refusal, Patients with pre-existing stenotic heart disease, Known case of eclampsia, Known case of neurological disorder, History of allergy to local anaesthetics, Contraindications to spinal anaesthesia, Patients with history of bleeding disorders or on anticoagulant therapy, ASA grade IV/V.

结局指标

主要结局

parameters compared will be SBP,DBP,MAP,PR,RR and SPO2

时间窗: parameters measured every 2min till 10min,every 5min till 30min ,every 15min till the end of surgery and then hourly till 24hours

次要结局

  • Total dose of atropine required ,(Total dose of mephentermine required,)

研究者

发起方
BJMedical College and Civil Hospital Ahmedabad Government of Gujarat
申办方类型
Government medical college
责任方
Principal Investigator
主要研究者

Dr MD Imran

B.J. Medical College and Civil Hospital , Ahmedabad

研究点 (1)

Loading locations...

相似试验