跳至主要内容
临床试验/CTRI/2019/03/018103
CTRI/2019/03/018103尚未招募不适用

Comparative study between Erector spinae plane block and Transversus abdominis plane block for postoperative analgesia in lower segment caesarean deliveries - A randomised control study

Kasturba Medical College student research fund1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2019年1月4日最近更新:
适应症

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
a)Duration of analgesia (by noting down the demand for first analgesia)

研究概览

简要总结

Caesareandelivery is one of the most commonly performed surgical procedures. Thepostoperative pain associated with it causes significant reduction in thefunctional quality of the postpartum mother especially on the day of theprocedure. The optimum form of postoperative analgesia is not known, but manyprocedures are carried out under spinal anaesthesia and patients typicallyreceive spinal opioids, systemic opioids as components of multimodal analgesiain the postoperative period. However, long acting opioids, whether given viathe spinal or systemic route, are frequently associated with adverse effectssuch as nausea, pruritus, sedation and occasionally respiratory depression.Thus knowledge about the alternative (non-opioid) analgesia especially regionaltechniques is important.

The regional techniques like epidural and TAP blockshave been found to provide effective postoperative analgesia in cesareandeliveries. ESP block is a novel technique which has found its applicability inmany truncal and hip surgeries. Also, it is believed that this technique istechnically less demanding as compared to other techniques described above

研究设计

研究类型
Interventional
分配方式
Computer generated randomization
盲法
Participant, Investigator, Outcome Assessor and Date-entry Operator Blinded

入排标准

年龄范围
18.00 Year(s) 至 40.00 Year(s)(—)
性别
Female

入选标准

  • •All ASA II pregnant women in the age group of 18 to 40 years undergoing elective lower segment caesarean deliveries under subarachnoid block are included in the study.

排除标准

  • •Patient refusal Coagulation disorders Local infection at the site of block Allergy to study medications BMI >35 kg/m2.

结局指标

主要结局

a)Duration of analgesia (by noting down the demand for first analgesia)

时间窗: Every hour for the first 10 hours and 24 hrs postoperatively

b)24 hour opioid (tramadol) consumption

时间窗: Every hour for the first 10 hours and 24 hrs postoperatively

次要结局

  • Patient satisfaction score from 1 to 10(24hours after the surgery)

研究者

发起方
Kasturba Medical College student research fund
申办方类型
Private medical college

研究点 (1)

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