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临床试验/CTRI/2024/08/072249
CTRI/2024/08/072249尚未招募不适用

A comparative study of epidural bupivacaine vs epidural ropivacaine for the relief of post operative pain in lower limb surgeries and lower abdominal surgries

Dr Swati Deswal1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2024年9月5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
100
试验地点
1
主要终点
To Compare the post operative analgesic effect after administration of epidural bupivacaine 0.125% and ropivacaine 0.1%

研究概览

简要总结

The Study â€œA Comparative Study Of Epidural Bupivacaine Vs Epidural Ropivacaine For The Relief Of Post Operative Pain In Lower Limb Surgeries And Lower Abdominal Surgries” will be conducted in Department of Anesthesia ,Varun Arjun Medical College and Rohilkhand Hospital, Banthra, Shahjahanpur, Uttar Pradesh 242307                                                                                                                                                                                                                                                        

A. The study will be conducted on subjects undergoing Lower Limb and Lower Abdominal Surgeries presenting to PAC Room in Department of Anesthesia ,Varun Arjun Medical College and Rohilkhand Hospital, Banthra, Shahjahanpur based on Inclusion and Exclusion criterias

B. All patients selected for the study will undergo datailed history taking and written informed consent

C. PAC assessment

D. Laboratory assessment

E. Patients will be admitted one day before the surgery

F. Patients will be allocated randomly into 2 groups

Group A : Patients in this group will receive a 0.125% Bupivacaine infusion in the post-operative recovery room

Group B : Patients in this group will receive a 0.1% Ropivacaine infusion in the post-operative recovery room

G. Patient Monitoring : SBP, DBP, MAP, HR and VAS SCORE recorded at specified intervals after starting epidural infusion for the first 24 hours

H. Adverse Events : Any adverse events , such as cardiac toxicity and motor blockade and other side effects , will be recorded

研究设计

研究类型
Interventional
分配方式
Other
盲法
None

入排标准

年龄范围
18.00 Year(s) 至 65.00 Year(s)(—)
性别
All

入选标准

  • American Society of Anesthesiologists ASA physical status I-II Except Pregnant or Lactating women Informed consent will be obtained from the patients for participating in the study.

排除标准

  • Patients with known allergies to Local Anesthesia Patients with contraindications to epidural anesthesia For example infection at the injection site and coagulopathy Patients with chronic pain conditions or on longterm opioid therapy Patients with neurological or psychiatric conditions that may interfere with pain assessment.

结局指标

主要结局

To Compare the post operative analgesic effect after administration of epidural bupivacaine 0.125% and ropivacaine 0.1%

时间窗: From starting of infusion till 24 hours

次要结局

  • To Determine the requirement for rescue analgesia postoperatively when patient is on Epidural infusion(From starting of infusion till 24 hours)

研究者

发起方
Dr Swati Deswal
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

Dr Swati Deswal

Varun Arjun Medical College and Rohilkhand Hospital

研究点 (1)

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