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临床试验/NCT07460115
NCT07460115已完成不适用

Comparison of Mean Duration of Analgesia Following the Administration of Bupivacaine With and Without Magnesium Sulphate in Ultrasound Guided Erector Spinae Plane Block in Modified Radical Mastectomy Patients

Gulab Devi Hospital1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2025年5月28日最近更新:
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
60
试验地点
1
主要终点
post-operative analgesia

研究概览

简要总结

To compare mean duration of postoperative analgesia following the administration of bupivacaine with and without magnesium sulphate in erector spinae plane block in modified radical mastectomy patients.

详细描述

There is a difference in mean duration of analgesia following the administration of bupivacaine with and without magnesium sulphate in erector spinae plane block in modified radical mastectomy patients.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Participant)

入排标准

年龄范围
25 Years 至 60 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Female patients having ASA 1 and Il being aged 2 5 - 60 years and undergoing one sided breast cancer surgery * Patients who sign written informed consent to participate in the study.

排除标准

  • Patients having contraindications for regional blocks (c.g., infection a t the injection site, coagulopathy), allergy to the drugs used i n the study Patients who received radiotherapy, and patients need axillary dissection • Patients with known hypersensitivity to local anesthetic drug (Bupivacaine). Patients with coagulation disorders or receiving anti-coagulant therapy (INR>2.0).

研究组 & 干预措施

Group bupivacaine

Active Comparator

20 ml of 0.25% bupivacaine

干预措施: Group B (bupivacaine) (Drug)

Group BMG(bupivacaine plus magnesium sulfate)

Experimental

20 ml of 0.25% bupivacaine plus 250 mg of magnesium sulfate

干预措施: Bupivacaine plus magnesium sulfate (Drug)

结局指标

主要结局

post-operative analgesia

时间窗: 20 minutes

There is a difference in mean duration of analgesia following the administration of bupivacaine with and without magnesium sulphate in erector spinae plane block in modified radical mastectomy patients.

次要结局

未报告次要终点

研究者

发起方
Gulab Devi Hospital
申办方类型
Other
责任方
Principal Investigator
主要研究者

Fareeha Afzaal

Post Graduation Resident

Gulab Devi Hospital

研究点 (1)

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