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临床试验/CTRI/2024/07/070112
CTRI/2024/07/070112尚未招募4 期

Comparative Study Of Efficacy Of Intrathecal FentanylBupivacaine And Tramadol-Bupivacaine Combination With Bupivacaine Normal For Infraumbilical Surgeries: A Double Blind Randomized Control Trial - Nil

Dr Tanya Sethi0 个研究点目标入组 0 人开始时间: 待定最近更新:

试验速览

阶段
4 期
状态
尚未招募
发起方

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

入选标准

  • 1. All patients posted for elective infra-umbilical surgeries (with duration of surgery =2 hours).
  • 2. Age of the patient between 15-70 years.
  • 3. Weight of the patient between 30-70 kg.
  • 4. Patients belonging to ASA class I and II.

排除标准

  • 1. Duration of surgery more than 2 hours
  • 2. Patients belonging to ASA class III and IV.
  • 3. Patients with coagulation disorders.
  • 4. Patients with infection at the site of block.
  • 5. Patients with vertebral column deformities, spinal cord deformity, or any neurological deficit
  • 6. Patients with psychiatric disorders.
  • 7. Pregnant patients.
  • 8. Patients with history of hypersensitivity to any of the drugs under study.
  • 9. Patients with uncontrolled hypertension or any decompensated cardiovascular disease.

研究者

发起方
Dr Tanya Sethi

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