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临床试验/CTRI/2025/08/093277
CTRI/2025/08/093277尚未招募Phase 3 4

A randomized interventional trial. Comparative assessment of pain relief by ultrasound guided tender point blockade vs ilioinguinal nerve block in chronic pain post herniorrhaphy

DR SN MEDICAL COLLEGE1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2025年9月5日最近更新:

试验速览

阶段
Phase 3 4
状态
尚未招募
发起方
入组人数
50
试验地点
1
主要终点
The primary outcome is post procedure pain assessment by VAS Pain assessment scales

研究概览

简要总结

**Herniorrhaphy postoperative pain prevention includes preoperative and intraoperative local anaesthetic infiltration field blocks paravertebral blocks  tender point blockade and NSAIDs or COX 2 inhibitors preoperative or intraoperative field blocks mainly targeting the ilio-inguinal nerve with or without wound infiltration are more effective than placebo or no treatment for reducing early postoperative pain and reducing the need for additional analgesics.**Tender point blockade with 10 ml 0.25% ropivacaine which involves targeting specific areas of muscle or nerve irritation, can also provide relief by addressing localized pain. It has been found to reduce pain and muscle tenderness previously, particularly in patients with myofascial pain after surgery. The technique can be integrated with other pain management approaches, such as local anaesthetic infiltration and nerve blocks, to enhance overall pain control in the post herniorrhaphy chronic pain of 6  months or more and comparing it with ilioinguinal nerve block with 10 ml 0.25% ropivacaine.

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 60.00 Year(s)(—)
性别
All

入选标准

  • Patient who underwent herniorraphy surgery having pain for more than 6 months with intensity of more than 5 by VAS.

排除标准

  • Patient who are having recurrent inguinal hernia 2)Allergy to local anaesthetics 3)Infection in wound area 4)Drug abuse.

结局指标

主要结局

The primary outcome is post procedure pain assessment by VAS Pain assessment scales

时间窗: 0 minutes, 10 minutes, 1 week, 1 month

次要结局

  • Pain assessment using other pain scales post blockade(0 minutes, 10 minutes, 1 week, 1 month)

研究者

发起方
DR SN MEDICAL COLLEGE
申办方类型
Government medical college
责任方
Principal Investigator
主要研究者

Dr Shikha Soni

DR SN MEDICAL COLLEGE

研究点 (1)

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