相关临床试验
26
10 进行中
药物批准
0
批准总数
监管机构
0
监管机构数
成立时间
1870
已完成
11
42.3%
尚未招募
10
38.5%
招募中
3
11.5%
终止
2
7.7%
暂无批准数据
- Sentec's LuMon™ Electrical Impedance Tomography system becomes the first EIT technology cleared by FDA for premature infants and spontaneously breathing patients in the United States. - The radiation-free bedside imaging system provides real-time visualization of lung function to help clinicians personalize ventilatory care for critically ill neonatal patients. - The technology addresses a significant clinical need in NICUs where ventilation management errors can have lifelong consequences for premature infants. - The system features soft fabric belts designed specifically for very low birthweight infants and delivers continuous monitoring of regional lung function.
- Three pioneering pilot randomized controlled trials (CASCADE Junior) launched to evaluate effectiveness of various central venous access device securement methods in pediatric patients. - Study compares innovative technologies including tissue adhesive, integrated securement dressings, and sutureless securement devices against conventional methods for different CVAD types. - Research aims to reduce the 25% failure rate of pediatric CVADs and prevent serious complications including catheter-associated bloodstream infections, which carry up to 35% mortality risk.