跳至主要内容
临床试验/CTRI/2025/06/088553
CTRI/2025/06/088553尚未招募不适用

COMPARISON OF FRACTIONATED DOSE WITH BOLUS DOSE OF 0.5 PERCENT HYPERBARIC BUPIVACAINE IN SPINAL ANAESTHESIA FOR PATIENTS UNDERGOING CAESAREAN SECTION

Priyanka kaushik1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2025年6月20日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
60
试验地点
1
主要终点
Severity of pain assessment using VAS pain score and modified bromage scale

研究概览

简要总结

This study is a comparative randomised observational study of fractionated with bolus dose of 0.5% hyperbaric bupivacaine in spinal anaesthesia for patients undergoing caesarean section. The comparison between fractionated and bolus doses of hyperbaric bupivacaine in spinal anesthesia for cesarean section involves evaluating their effects on both maternal and fetal outcomes, as well as the quality of anesthesia, side effects, and duration of action. Total 60 patients will be randomly selected which belongs to ASA I -III. 60 patients will be divided into two groups 30 in each by using sealed envelope technique. One group will receive drug as bolus and other will receive drug as fractionated and drug will be given to pregnant females via spinal anaesthesia under all aseptic precautions.

研究设计

研究类型
Interventional
分配方式
Coin toss, Lottery, toss of dice, shuffling cards etc
盲法
Participant and Investigator Blinded

入排标准

年龄范围
21.00 Year(s) 至 36.00 Year(s)(—)
性别
Female

入选标准

  • Physical status I-III according to American Society of Anaesthesiologist 2) Singleton live pregnancies more than 37 weeks of gestation for elective or emergency caesarean 3) Body mass index less than 30.

排除标准

  • Patients wit pre-existing diseases like cardiovascular or cerebrovascular disease or pregnancy induced hypertension 2) Severely altered mental status 3)Spinal deformities 4) History of laminectomy 5) Any contraindication to spinal anaesthesia 6) Emergency caesarean section who cannot be explained about the study due to paucity of time.

结局指标

主要结局

Severity of pain assessment using VAS pain score and modified bromage scale

时间窗: 2,4,6,8,10,15,20,30,40,50 and 60 mins

次要结局

  • 1) Hemodynamic parameters variations(2) Block characteristics)

研究者

发起方
Priyanka kaushik
申办方类型
Other [self]

研究点 (1)

Loading locations...

相似试验