EUCTR2017-001011-36-FR进行中（未招募）1 期
Multicentric, comparative, randomized, open study comparing an early post-operative prophylactic non-invasive ventilation (NIV) to standard post-operative care in patients at high-risk of respiratory complications according to ARISCAT preoperative scoring system whose surgery is performed under general or loco-regional anesthesia (ANTICIPUSC).
INSTITUT DE CANCEROLOGIE DE L'OUEST0 个研究点目标入组 266 人开始时间: 2017年3月28日最近更新:
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
- 266
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
入选标准
- •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 86
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 180
排除标准
- 未提供
研究者
相似试验
已完成
不适用
MULTICENTRIC, OPEN, RANDOMIZED, COMPARATIVE STUDY TO EVALUATE THE EFFICACY AND SAFETY OF TELITROMYCIN 800 MG VIA ORAL ONCE A DAY FOR 5 DAYS VS. AMOXICILLINE / CLAVULIC ACID 500/125 MG VIA ORAL THREE TIMES A DAY FOR 10 DAYS IN THE TREATMENT OF ACUTE MAXILAR SYNTHETIS OR MAXILAR-ACUTE ETHIOIDAL IN ADULTS.PER-040-02AVENTIS PHARMA S.A.,
尚未招募
不适用
Study of efficacy and safety of FormairCTRI/2017/01/007711Rus Biopharm150
进行中（未招募）
不适用
An open, randomised, comparative, multicentre study of the immunogenicity and safety of concomitant versus separate administration of a combined measles, mumps, rubella and varicella live vaccine (ProQuad®) and a booster dose of Infanrix® hexa in healthy children 12 to 23 months of age.EUCTR2006-004129-27-DESanofi Pasteur MSD960
进行中（未招募）
不适用
An open, randomised, comparative, multicentre study of the immunogenicity and safety of M-M-R™II manufactured with recombinant Human Albumin (rHA) and VARIVAX® when administered concomitantly by intramuscular (IM) route or subcutaneous (SC) route at two separate injection sites in healthy subjects 12 to 18 months of age - MMR rHA + VARIVAX IM or SC in 12-18 month-old healthy subjectsot applicable - Healthy subjectsEUCTR2004-002586-21-DEAventis Pasteur MSD SNC700
进行中（未招募）
不适用
Open, Randomised, Comparative, Multicentre Study of the Immunogenicity and Safety of Concomitant versus Separate administration of a combined measles, mumps, rubella and varicella live vaccine ProQuad and a Booster dose of Infanrix hexa in Healthy Children 12 to 23 months of age - X06-MMRV-302EUCTR2006-004129-27-ITCASA MADRE960