跳至主要内容
临床试验/CTRI/2023/05/052407
CTRI/2023/05/052407尚未招募不适用

To Compare Bupivacaine vs Bupivacaine-Dexamethasone in LSCS patients with Transverse abdominis plane block.

DR D Y PATIL MEDICAL COLLEGE HOSPITAL KOLHAPUR1 个研究点 分布在 1 个国家目标入组 176 人开始时间: 2023年5月23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
176
试验地点
1
主要终点
VAS SCORE will be assessed for the patients

研究概览

简要总结

THIS STUDY IS AN RANDOMISED DOUBLE BLIND ACTIVE CONTROLLED STUDY . WE ARE ASSESSING THE POST OPERATIVE ANALGESIC EFFECT AFTER GIVING TAP BLOCK WITH 2 DIFFERENT TYPE OF DRUGS FOR 2 DIFFERENT GROUP OF PATIENTS. FIRST GROUP IS GIVEN TAP BLOCK WITH INJ BUPIVACAINE 0.25 % + INJ DEXAMETHASONE AND SECOND GROUP IS GIVEN TAP BLOCK WITH INJ BPIVACAINE 0.25% PLAIN. POST OPERATIVELY BLOCK WAS GIVEN AND PAIN WAS ASSESSED USING VAS SCORE FOR 24 HOURS.

研究设计

研究类型
Interventional
分配方式
Computer generated randomization
盲法
Participant and Investigator 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

  • ALL LSCS PATIENTS UNDER SUBARACHNOID BLOCK.

排除标准

  • PATIENT REFUSAL 2) PATIENT WITH ASA GRADE III AND IV 3) LOCAL SKIN INFECTIONS( LATERAL ABDOMINAL WALL) 4) SIGNIFICANT CARDIAC DISEASE 5) SUSPECTED COAGULOPATHIES OR BLEEDING DISORDERS 6) ALLERGY TO LOCAL ANAESTHETICS AND STUDY DRUG.

结局指标

主要结局

VAS SCORE will be assessed for the patients

时间窗: It will be assessed at a 4hour interval upto 24 hours after giving the block.

次要结局

  • when the BREAKTHROUGH ANALGESIA is to be given for the patients.(until 24 hours after giving TAP block.)

研究者

发起方
DR D Y PATIL MEDICAL COLLEGE HOSPITAL KOLHAPUR
申办方类型
Research institution and hospital

研究点 (1)

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