跳至主要内容
临床试验/CTRI/2024/09/073900
CTRI/2024/09/073900尚未招募4 期

A Prospective Randomised Double Blind interventional Comparative study of administration of Ondansetron 8mg intravenous versus placebo before Spinal Anaesthesia in attenuation of post Spinal Hypotention at SMS Medical College, Jaipur

Department of Anaesthesia Sawai Maan Singh College and Attached Hospital Jaipur1 个研究点 分布在 1 个国家目标入组 174 人开始时间: 2024年9月20日最近更新:

试验速览

阶段
4 期
状态
尚未招募
发起方
入组人数
174
试验地点
1
主要终点
1.To determine the difference in fall of systolic blood pressure SBP (in mm Hg), diastolic pressure (DBP in mm Hg), mean arterial pressure(MAP) and heart rate (HR) between both groups.

研究概览

简要总结

Hypotension is seen in as many as 50% of the parturients undergoing lower segment caesarean section (LSCS) under spinal anaesthesia. Hypotension due to spinal anaesthesia is mainly caused by sympathetic blockade . In obstetric patients spinal anaesthesia induced hypotension is further aggravated due to aortocaval compression by gravid uterus. Many techniques such as lower legs compression, uterine displacement, using vasopressor and administering fluids has shown a decrease in incidence of hypotension.

In this study, we plan to study and compare the effect of 8mg intravenous (IV) ondansetron and placebo given prophylactically 5 minutes (min.) before spinal anaesthesia on incidence of hypotension in patients undergoing elective caesarean section.

For this study a total of 174 patients (n=174)  undergoing elective caesarean section who satisfy the inclusion criteria will be randomly divided into two groups of 87 each (n=87) (A and B),Group A will receive 8mg of IV ondansetron and group B will receive placebo 5min. before spinal anaesthesia .

When patient arrives in the operating room (OR), IV cannula will be inserted and haemodynamic variables will be measured. After this patient will receive 4mg of IV ondansetron (Group A) and 8mg of IV ondansetron  5min. before spinal anaesthesia. After this spinal anaesthesia will be administered. Patient will be put in supine position immediately. Surgery will be allowed to proceed after the block reaches T6 sensory level (complete sensory block). Quantitative values of ephedrine use (mg) and IV crystalloids (L) will be recorded.

Haemodynamic parameters including systolic blood pressure (SBP), diastolic blood pressure (DBP), mean arterial blood pressure (MAP), pulse rate (PR), oxygen saturation (SPO2), and respiratory rate (RR) will be recorded preoperatively and intraoperatively. The data will be collected in a prescribed proforma and statistically analysed.

研究设计

研究类型
Interventional
分配方式
Other
盲法
Participant and Investigator Blinded

入排标准

年龄范围
20.00 Year(s) 至 45.00 Year(s)(—)
性别
Female

入选标准

  • 1.Patient consenting to participate.
  • 2.Adult patients 3.Patient belonging to ASA grade II.

排除标准

  • 1.Patients with contraindication to neuraxial anaesthesia.
  • 2.Patient with history of drug abuse or addictions.
  • 3.SA converted to general anaesthesia.
  • 4.Allergy to ondansetron or local anaesthetic contraindication to regional anaesthesia and on medications which acts on the 5HT3 receptors were excluded from the study.

结局指标

主要结局

1.To determine the difference in fall of systolic blood pressure SBP (in mm Hg), diastolic pressure (DBP in mm Hg), mean arterial pressure(MAP) and heart rate (HR) between both groups.

时间窗: PRE OP | 00 (after spinal) | 01 min | 02 min | 03 min | 05 min | 10 min | 15 min | 20 min | 25 min | 30 min | 40 min | 50 min | 60 min

2.To determine difference in dose of ephedrine requirement in (mg) in both groups

时间窗: PRE OP | 00 (after spinal) | 01 min | 02 min | 03 min | 05 min | 10 min | 15 min | 20 min | 25 min | 30 min | 40 min | 50 min | 60 min

次要结局

  • 1.To observe side effects – if any(PRE OP)

研究者

发起方
Department of Anaesthesia Sawai Maan Singh College and Attached Hospital Jaipur
申办方类型
Government medical college
责任方
Principal Investigator
主要研究者

Dr Harpreet Kaur

Sawai Man Singh Medical College and Attached Hospitals

研究点 (1)

Loading locations...

相似试验