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.
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
研究点 (1)
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