NCT00845754已完成不适用
Effects of Ketorolac on Post-Operative Febrile Morbidity and Pain Management in Abdominal Myomectomy Patients
Ascher-Walsh, Charles, M.D.1 个研究点 分布在 1 个国家目标入组 112 人开始时间: 1999年9月最近更新:
适应症
干预措施
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 112
- 试验地点
- 1
- 主要终点
- Post-operative febrile morbidity
研究概览
简要总结
The purpose of this study is to determine if ketorolac, given after abdominal myomectomy, will decrease the frequency of post-oerative fevers as well as improve post-operative pain management.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- Double (Participant, Care Provider)
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- Female
- 接受健康志愿者
- 是
入选标准
- •Ant patient undregoing abdominal myomectomy
排除标准
- •Patients with contraindication to NSAIDs including history of peptic ulcer disease, renal disease, bleeding diathesis, or hypersensitivity to NSAIDS
研究组 & 干预措施
1
Placebo Comparator
Placebo
干预措施: saline (Drug)
2
Active Comparator
Ketorolac
干预措施: ketorolac (Drug)
结局指标
主要结局
Post-operative febrile morbidity
时间窗: Inital 24hrs post-operative
次要结局
- Post-operative pain management(Initial 24hrs post-operative)
研究者
研究点 (1)
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