跳至主要内容
临床试验/CTRI/2020/04/024687
CTRI/2020/04/024687尚未招募2/3 期

Analgesic efficacy of Inj. Dexamethasone as an adjuvant with Inj Levobupivacaine in ultrasound guided transverse abdominis plane (TAP) block after caesarean delivery- A prospective randomized controlled double blind study.

SSG Hospital1 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2020年4月20日最近更新:

试验速览

阶段
2/3 期
状态
尚未招募
发起方
SSG Hospital
入组人数
80
试验地点
1
主要终点
To compare the time to first rescue analgesia (Vas score 4) between the two groups.

研究概览

简要总结

Our goal is to evaluate the analgesic efficacy of Inj. Dexamethasone as adjuvant with Inj. Levobupivacaine as local anaesthetic in ultra sound guided transversus abdominis plane (TAP) block in post cesarean delivery conducted under spinal anaesthesia .Our primary objective is to compare the time to first rescue analgesia between the two groups determines by VAS (visual analogue scale) score of more than 4.

研究设计

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

入排标准

年龄范围
18.00 Year(s) 至 35.00 Year(s)(—)
性别
Female

入选标准

  • singleton ,full term pregnancy 2) ASA Physical status – I or II 3) scheduled for elective and emergency LSCS under spinal anaesthesia.

排除标准

  • Patients refusal and not able to understand study protocol.
  • Patients who are hypersensitivity to local anaesthetic drug.
  • Contraindication to spinal anaesthesia.
  • Severe PIH 5) Patients with compromised renal and liver function, uncontrolled diabetes severe cardiovascular and respiratory disease.
  • Infection, trauma, scar or sinuses at site of TAP block.

结局指标

主要结局

To compare the time to first rescue analgesia (Vas score 4) between the two groups.

时间窗: VAS Score at 2,4,6,8,12,18 and 24 hours.

次要结局

  • To compare the total amount of rescue analgesia required in first 24 h post operatively.
  • Hemodynamic parameter in both groups. [PR, BP, SPO2] post block(Baseline (just after shifted to USG room))

研究者

发起方
SSG Hospital
申办方类型
Government medical college

研究点 (1)

Loading locations...

相似试验