跳至主要内容
临床试验/CTRI/2023/01/049005
CTRI/2023/01/049005尚未招募未知

Comparison of Aprepitant, Dexamethasone and Ondansetron with Dexamethasone and Ondansetron for prevention of post operative nausea vomiting in high risk patients undergoing laparoscopic surgeries. A Randomised control trial.

AIIMS0 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
未知
状态
尚未招募
发起方
AIIMS

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

  • FEMALE >18 YRS,NON SMOKERS UNDERGOING LAPAROSCOPIC SURGERY LASTING 2-4 HOURS, RECEIVING INTRAOPERATIVE AND POSTOPERATIVE OPIOID ANALGESIA.

排除标准

  • 1. CONSUMPTION OF AN AGENT WITH ANTI EMETIC PROPERTIES WITHIN 24 HRS PRIOR TO COMMENCEMENT OF THE STUDY.
  • 2. KNOWN HYPERSENSITIVITY TO APREPITANT, ONDANSETRON OR DEXAMETHASONE.
  • 3. PREGNANCY.
  • 4. PATIENTS REQUIRING POSTOPERATIVE MECHANICAL VENTILATION.
  • 5. SURGERY LASTING >4 HRS
  • 7. PATIENTS NOT GIVING CONSENT.

研究者

发起方
AIIMS

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