跳至主要内容
临床试验/CTRI/2024/11/076655
CTRI/2024/11/076655尚未招募2 期

To assess the post-operative analgesic effect of single-shot ropivacaine versus ropivacaine with dexamethasone in adductor canal block for knee surgeries.

Dr Abha Agnihotri1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2024年11月22日最近更新:

试验速览

阶段
2 期
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 postoperative analgesic effect of Ropivacaine with normal saline and Ropivacaine with Dexamethasone after knee surgeries when given in ACB.Duration of analgesia that is duration between administration of block and first

研究概览

简要总结

The selected patients will either receive 30 ml of 0.2% ropivacaine with 2 ml of normal saline or 30 ml of 0.2% ropivacaine with 2 ml (8 mg) dexamethasone after completion of knee surgeries under spinal anaesthesia.

Pain will be assessed at different time intervals using VAS score and rescue analgesics will be given accordingly.

研究设计

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

入排标准

年龄范围
18.00 Year(s) 至 90.00 Year(s)(—)
性别
All

入选标准

  • Patients above the age of 18, under ASA grade I and II, undergoing uneventful knee surgeries and giving written informed consent to participate in the study will be included.

排除标准

  • 1.Patients below the age of
  • 2.Pregnant women.
  • 3.Rashes on the site of procedure.
  • 4.Bleeding disorders.
  • 5.Uncontrolled hypertension, bradycardia, on beta-blockers or history of any cardiovascular diseases.
  • 6.Psychiatric illness.
  • 7.Patient on any chronic medication.
  • 8.History of hypersensitivity to local anaesthetics.
  • 9.All patients included in ASA grading III & IV.

结局指标

主要结局

To compare the postoperative analgesic effect of Ropivacaine with normal saline and Ropivacaine with Dexamethasone after knee surgeries when given in ACB.Duration of analgesia that is duration between administration of block and first

时间窗: 0, 6, 12, 18, 24 and 48 hrs.

rescue analgesic.

时间窗: 0, 6, 12, 18, 24 and 48 hrs.

次要结局

  • To compare requirement of post-surgery rescue analgesic after using visual acuity(score)

研究者

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

Dr Abha Agnihotri

Maharishi Markandeshwar Medical College and Hospital, Kumarhatti Solan

研究点 (1)

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