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临床试验/CTRI/2024/11/076122
CTRI/2024/11/076122尚未招募4 期

Comparison of Transversalis Fascia Plane Block with Quadratus Lumborum Block for Postoperative Analgesia After Laparoscopic Abdominal Hysterectomy

Teerthanker Mahaveer Medical College and Research Centre1 个研究点 分布在 1 个国家目标入组 90 人开始时间: 2024年11月18日最近更新:

试验速览

阶段
4 期
状态
尚未招募
发起方
入组人数
90
试验地点
1
主要终点
To compare total consumption of analgesics in 24 hours postoperatively.

研究概览

简要总结

After getting approval from Institutional Ethical Committee (IEC) ,those patients who are fit in inclusion criteria will be included in our study.

Two groups both including 45 patients will be created and randomization will be done by computer method.

General Anaesthesia will be given as per the institution’s protocol.

•After Surgery before Extubation.

•Group QL-Quadratus lumborum  25ml of 0.5% Ropivacaine

•Group TF- Transversalis fascia plane block 25ml of 0.5% Ropivacaine.

The patient will be shifted to PACU and standard analgesia (1 gm PCM 8 hourly i/v) will be given as per standard institute protocol.

VAS score and hemodynamic parameters will be recorded at the end of surgery immediately after block 15mins, 30 mins, 45mins, 1hr, 2hr, 4hr, 8hr,then after 12hr, and 24hr

•VAS >4 will be given rescue analgesia in form of I/V Tramadol 1gm/kg body weight.

•Total rescue analgesic consumption in 24 hrs and complications will be noted.

•Data will be analyzed using the appropriate statistical method.

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 65.00 Year(s)(—)
性别
All

入选标准

  • Patient posted for elective Laparoscopic Hysterectomy giving written and informed consent .
  • Age between 18 and 65Â yrs.
  • American society of anesthesiologist (ASA) physical status I-II.

排除标准

  • BMI more than 35kg/m2 history of coagulopathy history of chronic opiate abuse/alchol abuse pre existing chronic pain allergy to LA infection at injection site.

结局指标

主要结局

To compare total consumption of analgesics in 24 hours postoperatively.

时间窗: To compare total consumption of analgesics in 1hr,2hr,3hr subsquently every 1hr total 24hr duration

次要结局

  • To compare duration of first rescue analgesia.

研究者

发起方
Teerthanker Mahaveer Medical College and Research Centre
申办方类型
Private medical college
责任方
Principal Investigator
主要研究者

Dr Anamika Kumari

TMU MEDICAL COLLEGE AND HOSPITAL MORADABAD

研究点 (1)

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