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临床试验/CTRI/2019/08/020888
CTRI/2019/08/020888已完成4 期

Comparision of intraperitoneal dexamethasone, dexmedetomidine and dexamethasone-dexmedetomidine combination on postoperative nausea and vomiting and analgesics requirement after gynecological laparoscopy: a randomized clinical trial

Apollo Hospitals Bilaspur1 个研究点 分布在 1 个国家目标入组 160 人开始时间: 2019年2月9日最近更新:

试验速览

阶段
4 期
状态
已完成
入组人数
160
试验地点
1
主要终点
Incidence of post operative nausea and vomiting

研究概览

简要总结

Postoperative nausea and vomiting is common, but distressing complaint following general anesthesia. The PONV incidence as high as 60% to 80% in high risk patients when no prophylactic antiemetics used.

In this modern era of surgery intraperitoneal instillation of drugs has become an important method to control postoperative nausea and vomiting and decrease the analgesic requirement. Intraperitoneal dexamethasone and dexmedetomidine has been used separately for prevention of PONV. However, there is no study to compare the effectiveness of these drugs alone or in combination for prevention of PONV and analgesic requirement via intraperitoneal route.

All selected patients will be randomized in to 4 groups (40 in each group) depending on the drug given

Group D1 -  received dexamethasone 8 mg intraperitoneally at the end of the procedure, before laparoscopic trocar withdrawal, in total volume of 20 ml

Group D2 - received dexmedetomidine 1 mcg/kg intraperitoneally at same time and same volume

Group D3 - received dexamethasone 8 mg and dexmedetomidine 1 mcg/kg at the same time and same volume

Group D4 - receive 20 ml normal saline at the same time

Primary outcome - incidence of post operative nausea and vomiting

Secondary outcome - Total paracetamol requirement in 24 hr post operative period

Statistical analysis will be done after completion of study

研究设计

研究类型
Interventional
分配方式
Computer generated randomization
盲法
Participant, Investigator and Outcome Assessor Blinded

入排标准

年龄范围
30.00 Year(s) 至 60.00 Year(s)(—)
性别
Female

入选标准

  • ASA grade I and II
  • Scheduled for laparoscopic gynaecological surgery under general anesthesia.

排除标准

  • 1.Known allergy to study drugs 2.Use of antiemetic drugs within 24 hours of surgery 3.Morbid obesity( body mass index>40) 4.Chronic use of opioids 5.Patients with hepatic, renal or cardiovascular dysfunction 6.Psychiatric patients.

结局指标

主要结局

Incidence of post operative nausea and vomiting

时间窗: 24 hr postoperatve period

次要结局

  • Total consumption of paracetamol(24 hr postoperative period)

研究者

申办方类型
Research institution and hospital

研究点 (1)

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