Comparative evaluation of spinal anesthesia between 0.5% Levobupivacaine and 0.5% Ropivacaine for open hernia surgeries -A Randomized Prospective Study
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- 入组人数
- 50
- 试验地点
- 1
- 主要终点
- Duration of analgesia
研究概览
简要总结
Introduction:
Spinal anaesthesia is routinely used for lower umblical procedures.Bupivacaine 0.5%heavy is routinely used .Recently levobupivacaine is introduced .it has more cardio stability.I BETWEEN n this study we are comparing spinal anaesthesia effect isobaric 0.5% Levobupivacaine and isobaric 0.5% Ropivacaine
Aim:
To compare the clinical effect and quality of spinal isobaric 0.5% Levobupivacaine and isobaric 0.5% Ropivacaine for elective open hernia surgeries
Primary objective
To compare the time of onset of sensory block,
To compare the time to peak sensory block
To observe the differences in the duration of sensory block
To determine the duration of analgesia
Secondary objective
To observe and compare the hemodynamic instability
To identify the complications developing if any
CENTRE : Stanley medical college hospital, Chennai
DURATION : 6 months
DESIGN : A Randomised , Prospective study
POPULATION : Patients coming for Elective open hernia surgeries
SAMPLE SIZE : 50
Based on the reference study done by Samar et al, Mumbai
Formula:
n = 2 (Za+ZB)2 SD2 / (M1-M2)2
Where Za = 1.96 (statistical significant constant for 95% CI) , ZB = 0.84 (80% power)
Sd = 1.82 (Standard deviation of onset of sensory block in minutes among patients belonging to levobupivacaine group from previous study. )
M1 =8.47 (Mean onset of sensory block in minutes among patients belonging to ropivacaine group from previous study.M2 = 6.97 (Mean onset of sensory block in minutes among patients belonging to levobupivacaine group from previous study.)
(M1-M2)2 = 2.25 (1.5 x 1.5)On substituting in the formula.n = 15.6 x 1.8 x 1.8 / 2.25 ;n = 22
Adding 10% non response rate (ie 10% of 22= 2)n = 24 (minimum sample size).Therefore Sample size n = 25 (1 group) n = 50 (2 groups).
Methodology:
After ethical committee clearance and getting informed written consent fifty patients will be equally divided into two groups INCLUSION CRITERIA
• American society of anaesthesiologist physical status I & II
Age between 20 – 60 years
Posted for elective open hernia surgery
Patients willing to participate
EXCLUSION CRITERIA
American society of anaesthesiologist physical status III & IV
Coagulation Abnormalities
Localised Infections
Severe renal,hepatic,& cardiovascular diseases
Patients not willing for spinal anaesthesia
Group A: Contains 25 patients will receive spinal anaesthesia with 2.0 ml 0.5 % Levobupivacaine
Group B: Contains 25 patients will receive spinal anaesthesia with 2.0 ml 0.5 % Ropivacaine
Randomization will be done using computer generated random numbers and allocation will be done using sealed envelope technique. Intravenous line will be secured and crystalloids connected.standars monitors like pulse oximeter,Non invasive blood pressure and Electro cardio gram will be connected. Sub arachnoid block will be given using quincke needle at L3-4 level with patient in sitting position. Patient, investigator and statistician will be blinded to the study drug as drug will be prepared by an anaesthesiologists who is not involved in the study.
Heart rate,systolic and diastolic blood pressure and saturation will be monitored every 3miutes for first 10minutes then every 15 minutes till the end of the surgery
Sensory block – pin prick test, 24g hypodermic needle – every 3 minutes initial 15 minutes then every 20 minutes
T10- L1 – surgical dermatome
Time of onset, time to achieve peak sensory level, duration of analgesiaHypotension, bradycardia, vomiting, desaturation, difficulty in breathing – appropriately managed
Level inadequate/ breakthrough pain / prolonged surgical time – GA given
Statisytical analysis: descriptive analysis of the data will be done .mean and standard deviation will be compared using student t test for normally distributed continuous variable and chi square test for discrete variable
研究设计
- 研究类型
- Interventional
- 分配方式
- Computer generated randomization
- 盲法
- Participant, Investigator and Outcome Assessor Blinded
入排标准
- 年龄范围
- 20.00 Year(s) 至 60.00 Year(s)(—)
- 性别
- All
入选标准
- •Posted for elective open hernia surgery Patients willing to participate.
排除标准
- •American society of anaesthesiologist physical status III & IV Coagulation Abnormalities Localised Infections Severe renal,hepatic,& cardiovascular diseases Patients not willing for spinal anaesthesia.
结局指标
主要结局
Duration of analgesia
时间窗: baseline,2,4,6,8,10min and every 10 mind till surgery finishes
次要结局
- hemodynamics and complications(time of giving drug into subarachnoid space to 8 hrs postoperative period)
