EUCTR2013-000290-73-ES进行中（未招募）不适用
Randomized, double-blind, phase IV trial comparing the efficacy of two methods of sedation in patients scheduled for outpatient diagnostic-therapeutic colonoscopy.
FUNDACION C.V. HOSPITAL PROVINCIAL DE CASTELLO0 个研究点开始时间: 2013年4月9日最近更新:
适应症
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
- 发起方
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
- All
入选标准
- •(1) Patient scheduled to undergo outpatient diagnostic-therapeutic colonoscopy who are referred from health centers in the province of Castellón.
- •(2) Age between 18 and 65 years of age.
- •(3) Informed consent signed prior to inclusion in the study.
- •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 278
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range 0
排除标准
- •(1) Refusal of the patient to participate in the study.
- •(2) Minors
- •(3) Pregnancy or lactation
- •(4) History of liver or kidney disease.
- •(5) History of psychotropic substance abuse
- •(6) Psychiatric illness
- •(7) Difficulty in communication with the patient for reasons of language or intellectual deficit.
- •(8) Bearded patients, due to difficulties in achieving a facial mask seal.
- •(9) Difficulty in placing the facial mask (facial injuries or malformations).
- •(10) Scheduled double exploration (gastroscopy and colonoscopy).
- •(11) Contraindication to any of the study drugs.
- •(12) Allergies to any of the components of the study drugs.
- •(13) Hemodynamic or respiratory instability or decompensation.
- •(14) Worsening of concomitant disease described in the basline visit.
研究者
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