跳至主要内容
临床试验/NCT02220361
NCT02220361Unknown4 期

Phase 4 Study of Effects of Dexmedetomidine on Prevention of Side Effects of Hemabate in Cesarean Section Patients

Jin Ni0 个研究点目标入组 120 人开始时间: 2014年9月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
发起方
入组人数
120
主要终点
vomiting

研究概览

简要总结

Hemabate is often used for gynecological patients. Hemabate is associated with many side effects, including a burning sensation in the stomach, nausea, vomiting, diarrhea etc. It is reported that dexmedetomidine reduce gastrointestinal reaction during perioperative period. We design this clinical trial to find if dexmedetomidine can prevent the side effects of hemabate in Cesarean Section patients.

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
Triple (Participant, Care Provider, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 40 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • gynecological patients

排除标准

  • Neuromuscular and endocrine diseases
  • Allergic reactions to a2-adrenergic agonist
  • Previous abdominal surgery including prior caesarean section.

研究组 & 干预措施

placebo group

Placebo Comparator

received 20 ml intravenous physiological saline

干预措施: placebo (Drug)

low dose dexmedetomidine group

Experimental

received 0.5μgkg-1 intravenous dexmedetomidine (Jiang Su Heng Rui Medicine Co. Ltd, Jiangsu Province, China) diluted to 20ml with physiological saline

干预措施: low dose dexmedetomidine (Drug)

hemabate+high dose dexmedetomidine group

Experimental

received 1μgkg-1 intravenous dexmedetomidine (Jiang Su Heng Rui Medicine Co. Ltd, Jiangsu Province, China) diluted to 20ml with physiological saline

干预措施: high dose dexmedetomidine (Drug)

结局指标

主要结局

vomiting

时间窗: 24h postoperatively

elevated blood pressure

时间窗: 24h postoperatively

fever

时间窗: 24h postoperatively

SpO2 Change

时间窗: participants will be followed for the duration of surgery, an expected average of 2 hours

nausea

时间窗: 24 h postoperatively

diarrhea

时间窗: 24h postoperatively

headache

时间窗: 24h postoperatively

systolic blood pressure and diastolic blood pressure change

时间窗: participants will be followed for the duration of surgery, an expected average of 2 hours

Heart rate change

时间窗: participants will be followed for the duration of surgery, an expected average of 2 hours

chest congestion

时间窗: 24h postoperatively

次要结局

未报告次要终点

研究者

发起方
Jin Ni
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Jin Ni

Department of Anesthesiology

Guangzhou Women and Children's Medical Center

相似试验