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临床试验/NCT02744495
NCT02744495已完成3 期

Prophylaxis of Postoperative Nausea and Vomiting After Cardiac Surgery (PONVACS)

Hôpital Privé de Parly II - Le Chesnay1 个研究点 分布在 1 个国家目标入组 502 人开始时间: 2016年2月最近更新:
适应症
干预措施

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
502
试验地点
1
主要终点
postoperative nausea and vomiting

研究概览

简要总结

To investigate the role of postoperative nausea and vomiting risk factors assessment after cardiac surgery. We designed a randomized controlled study comparing standard care (no risk factor assessment and no intervention) with prophylaxis of postoperative nausea and vomiting after cardiac surgery in high risk patients. Prophylaxis of postoperative nausea and vomiting by betamethasone (4mg) and/or droperidol (0.625mg) immediately after cardiac surgery, depending on risk factors (if risk score is over 2) in the intervention arm.

详细描述

Patients planned to undergo cardiac surgery were screened for inclusion. Inclusion criteria are as follow: Non emergent cardiac surgery; Age > 18 years; Affiliation to French Social Security; Approval of participation to the study; at the exclusion of: Pregnancy ; Contra indication to antiemetics; Chronic usage of antiemetics; and Emergent or complicated surgery.

Risk factors for postoperative nausea and vomiting were collected and patients were randomized by cluster into two arms.

Control: No prophylaxis whatever risk score is. Postoperative nausea and vomiting risk factors were not available for practicians.

Intervention: Preoperative collection of postoperative nausea and vomiting risk factors available for practicians. Prophylaxis if risk score is over 2. Prophylaxis of postoperative nausea and vomiting by betamethasone (4mg) and/or droperidol (0.625mg) immediately after cardiac surgery, depending on risk factors in the intervention arm.

All outcomes are assessed at 48 hours of surgery:

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Non emergent cardiac surgery
  • Age > 18 years
  • Affiliation to French Social Security
  • Approval of participation to the study

排除标准

  • Pregnancy
  • Contra indication to antiemetics
  • Chronic usage of antiemetics
  • Emergent or complicated surgery

研究组 & 干预措施

postoperative nausea and vomiting risk factors

Experimental

Preoperative collection of postoperative nausea and vomiting risk factors available for practicians.

干预措施: Betamethasone (Drug)

postoperative nausea and vomiting risk factors

Experimental

Preoperative collection of postoperative nausea and vomiting risk factors available for practicians.

干预措施: Droperidol (Drug)

结局指标

主要结局

postoperative nausea and vomiting

时间窗: 48hour

postoperative nausea and vomiting as a categorical variable

次要结局

  • number of postoperative nausea and vomiting(48hour)
  • postoperative nausea and vomiting (VAS)(48hour)
  • postoperative pain (VAS)(48hour)
  • postoperative discomfort (VAS)(48hour)
  • Antiemetics (treatment)(48hour)
  • Analgesics(48hour)
  • Side effects(48hour)
  • QTc interval(48hour)

研究者

发起方
Hôpital Privé de Parly II - Le Chesnay
申办方类型
Other
责任方
Principal Investigator
主要研究者

Sébastien CHAMPION

Dr

Hôpital Privé de Parly II - Le Chesnay

研究点 (1)

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