NL-OMON47573已完成4 期
Study protocol for a randomized clinical trial of a continuous butylscopolamine infusion versus a placebo in patients with a renal colic not responding to oral NSAIDs - BUSCOPA
适应症
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 入组人数
- 128
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
- 年龄范围
- 18 至 64(—)
入选标准
- •Legally capable and competent to understand the implications of participation in the study and signed informed consent
- •Age 18 years or older
- •presentation with renal colic confirmed by ultrasound or CT-scan, not responding to oral NSAIDs and therefore admitted to the urological ward for pain medication.
排除标准
- •Pregnancy or lactation
- •Known allergy to any of the products used
- •Contra-indication for NSAIDs
- •Diagnosis other than renal colic
- •Patients presenting with a temperature > 38.5°C at time of inclusion or <24 hours ago
- •Patients with antibiotic for UTI together with urolithiasis or urolithiasis with indication for drainage of the upper urinary tract
- •Any of the following conditions:
- •- Megacolon
- •- Intestinal mechanical stenoses
- •- Myasthenia gravis
- •- Untreated narrow angle glaucoma
- •- Epilepsy
- •- Alcohol or drugs intoxication
- •- Creatinin clearance < 30 ml/min
- •- Atrial fibrillation with heart rate > 100/min
- •- Ischemic heart disease
- •- Heart failure
- •- Severe aortic valve stenosis
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