EUCTR2008-003367-40-FR进行中(未招募)1 期
Pilot study of the effect of a substance P antagonist, aprepitant, on aldosterone and cortisol secretions in healthy volunteers - APHOS
CHU de Rouen0 个研究点目标入组 20 人开始时间: 2009年2月6日最近更新:
适应症
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 进行中(未招募)
- 发起方
- 入组人数
- 20
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- Male
入选标准
- •o Male subjects;
- •o Age ranging 18 - 30 years old;
- •o Submitted to a social security regimen;
- •o Agreeing to the study & Informed consent form signed;
- •o Body mass index (weight (kg)/height (m)²) < 27;
- •o No treatment received 6 weeks before inclusion;
- •o No anomaly after: complete clinical examination, pulse and blood pressure measurement, ECG;
- •o No biological abnormality after the following biological testing:
- •- Hematology: white & red blood cells & platelets count, haemoglobin, hematocrit
- •- Blood biochemistry: sodium, potassium, chloride, bicarbonate, creatinine, urea
- •- Urinary biochemistry (24 h collection): cortisol, aldosterone
- •- Serologies: HIV, HBV, HCV
- •o No participation in a clinical trial 3 months before inclusion.
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 20
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range
排除标准
- •Subject not agreeing to the study or impossible to follow-up; the persons in detention by judicial or administrative decision, patients hospitalized without consent, individuals admitted to a health or social facility for purposes other than research and legally protected adults or not in a position to express their consent.
- •Known history of significant medical or surgical pathology, notably endocrine;
- •Renal or hepatic insufficiency;
- •Nephrotic syndrome;
- •Edematous syndrome;
- •Hypertension or postural hypotension;
- •Cardiac rhythm or conduction pathologies;
- •Cardiac insufficiency;
- •Epilepsy;
- •Significant psychiatric disorder;
- •Known history of severe allergy, hypersensitivity to aprepitant and/or metoclopramide;
- •Hereditary problems of fructose intolerance, glucose-galactose malabsorption or sucrase-isomaltase deficit;
- •Impaired lactose tolerance.
研究者
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