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临床试验/CTRI/2026/03/106401
CTRI/2026/03/106401尚未招募2 期

Patient related outcome measures (PROMs) following splanchnic nerve neurolysis in the management of upper abdominal cancer pain -A Prospective observational study

Mounica K1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2026年4月15日最近更新:

试验速览

阶段
2 期
状态
尚未招募
发起方
入组人数
30
试验地点
1

研究概览

简要总结

This review describes fluoroscopy-guided splanchnic nerve block for managing severe abdominal cancer pain. It explains the anatomy, technique, and use of diagnostic blocks, neurolysis, and radiofrequency ablation. The procedure provides significant pain relief, reduces opioid use, and improves quality of life in refractory cases.

研究设计

研究类型
Interventional
分配方式
Na
盲法
None

入排标准

年龄范围
18.00 Year(s) 至 70.00 Year(s)(—)
性别
All

入选标准

  • 1.Age more than 18 years with intractable abdominal pain secondary to intra-abdominal malignancies 2.expected life expectancy more than 2 months 3.ability to give informed written consent 4.comply to follow up.

排除标准

  • 1.Age less than 18 yrs 2.surgically performed chemical splanchnicectomy 3.coagulopathy 4.local infection 5.known allergy to materials used.

研究者

发起方
Mounica K
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

Dr Mounica K

Institute of anaesthesiology madurai medical college

研究点 (1)

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