跳至主要内容
临床试验/JPRN-UMIN000006405
JPRN-UMIN000006405已完成未知

Randomized Double Blind Study to Evaluate the Efficacy of Droperidol Added to Patient-Controlled Epidural Analgesia with fentanyl for Prevention of Post-Operative Nausea and Vomiting in Subjects Undergoing Gynecologic Surgery - Randomized Double Blind Study to Evaluate the Efficacy of Droperidol Added to Patient-Controlled Epidural Analgesia with fentanyl for Prevention of Post-Operative Nausea and Vomiting in Subjects Undergoing Gynecologic Surgery

niversity of Yamanashi Hospital0 个研究点目标入组 150 人开始时间: 2011年10月7日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
150

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

年龄范围
20years-old 至 ot applicable(—)
性别
Female

入选标准

  • 未提供

排除标准

  • Those have known hypersensitivity to any drugs that is part of this study protocol, contraindications to epidural anesthesia, current opioid use, inability to use the PCEA device, alcohol or narcotic dependence, renal or hepatic insufficiency, QT elongation (QTc interval >450 ms) on preoperative electrocardiogram (ECG) assessment, Parkinsonism, demand premedication, a history of operations under combined general-epidural anesthesia, and a history of severe PONV.

研究者

发起方
niversity of Yamanashi Hospital

相似试验

进行中(未招募)
不适用
Examination of effictiveness of iron containing infusion in preventing anemia after heart surgery in childre
EUCTR2014-002107-16-ATGeneral Hospital Linz
进行中(未招募)
不适用
Randomized double blind trial to evaluate the efficacy and safety of dronedarone (400 mg BID) versus amiodarone (600 mg daily for 28 days then 200 mg daily thereafter) for at least 6 months for the maintenance of sinus rhythm in patients with atrial fibrillation (AF) - DIONYSOSMedDRA version: 9.1Level: LLTClassification code 10003658Term: Atrial fibrillationAtrial Fibrillation
EUCTR2006-005804-15-DEsanofi-aventis recherche & développement472
进行中(未招募)
不适用
Randomized double blind trial to evaluate the efficacy and safety of dronedarone (400 mg BID) versus amiodarone (600 mg daily for 28 days then 200 mg daily thereafter) for at least 6 months for the maintenance of sinus rhythm in patients with atrial fibrillation (AF) - DIONYSOSMedDRA version: 9.1Level: LLTClassification code 10003658Term: Atrial fibrillationAtrial Fibrillation
EUCTR2006-005804-15-CZsanofi-aventis recherche & développement472
进行中(未招募)
1 期
Randomized double blind trial to evaluate the efficacy and safety of dronedarone (400 mg BID) versus amiodarone (600 mg daily for 28 days then 200 mg daily thereafter) for at least 6 months for the maintenance of sinus rhythm in patients with atrial fibrillation (AF) - DIONYSOSMedDRA version: 9.1Level: LLTClassification code 10003658Term: Atrial fibrillationAtrial Fibrillation
EUCTR2006-005804-15-PLsanofi-aventis recherche & développement472
进行中(未招募)
不适用
Randomized double blind trial to evaluate the efficacy and safety of dronedarone (400 mg BID) versus amiodarone (600 mg daily for 28 days then 200 mg daily thereafter) for at least 6 months for the maintenance of sinus rhythm in patients with atrial fibrillation (AF) - DIONYSOSAtrial Fibrillation
EUCTR2006-005804-15-FIsanofi-aventis recherche & développement472