CTRI/2011/06/001850已完成2 期
A RANDOMIZED CONTROL TRIAL OF KETAMINE-PROPOFOL AND FENTANYL-PROPOFOL COMBINATION FOR PROCEDURAL SEDATION AND ANALGESIA (PSA) IN LAPAROSCOPIC TUBAL LIGATION?
lady hardinge medical college and S S K Hospital university of delhi1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2009年1月11日最近更新:
适应症
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 发起方
- 入组人数
- 100
- 试验地点
- 1
- 主要终点
- Measures patient recovery time and discharge time using Ketamine-Propofol And Fentanyl-Propofol Combination For PSA In Laparoscopic Tubal Ligation.
研究概览
简要总结
A randomized control trial of ketamine-propofol and fentanyl-propofol combination for procedural sedation and analgesia in laparoscopic tubal ligation in ASA physical status I patients aged 18-45 years female. primary outcome measures Perioperative Hemodynamic Changes Using Ketamine-Propofol And Fentanyl-Propofol Combination For PSA In Laparoscopic Tubal Ligation. secondary outcome measures Postoperative Recovery And Duration Of Hospital Stay And Comfort And Acceptability In The Two Groups
研究设计
- 研究类型
- Interventional
- 分配方式
- Computer generated randomization
- 盲法
- Investigator Blinded
入排标准
- 年龄范围
- 18.00 Year(s) 至 45.00 Year(s)（—）
- 性别
- Female
入选标准
- •Inclusion Criteria- American Society of Anesthesiologist physical status I patients aged 18-45 years female scheduled for laparoscopic tubal ligation.
- •Exclusion Criteria- history of upper respiratory tract infections, asthma, allergy to propofol or ketamine, receiving treatment for psychiatric disease, receiving treatment for neuromuscular disease, seizure disorder, acid reflux, hiatus hernia, severe anemia, gross obesity, hepatic,cardiac or pulmonary disease.
排除标准
- •Inclusion Criteria- American Society of Anesthesiologist physical status I patients aged 18-45 years female scheduled for laparoscopic tubal ligation.
- •Exclusion Criteria- history of upper respiratory tract infections, asthma, allergy to propofol or ketamine, receiving treatment for psychiatric disease, receiving treatment for neuromuscular disease, seizure disorder, acid reflux, hiatus hernia, severe anemia, gross obesity, hepatic,cardiac or pulmonary disease.
- •Patients who have history of upper respiratory tract infections, asthma or allergy to propofol or ketamine or receiving treatment for any psychiatric or neuromuscular disease, patients with seizure disorder, acid reflux, hiatus hernia, severe anemia, gross obesity, hepatic, cardiac, or pulmonary diseases will be excluded from this study.
结局指标
主要结局
Measures patient recovery time and discharge time using Ketamine-Propofol And Fentanyl-Propofol Combination For PSA In Laparoscopic Tubal Ligation.
时间窗: November 2009 to March 2011
次要结局
- postoperative recovery and duration of hospital stay and comfort and acceptability in the two groups(postoperative recovery and duration of hospital stay and comfort and acceptability in the two groups)
研究者
研究点 (1)
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