跳至主要内容
临床试验/DRKS00024819
DRKS00024819已完成未知

Prospective, monocentric clinical study about the effect of a novel technique for mucus mobilization on lung function, mucus viscosity and diaphragmatic mobility in cystic fibrosis patients - SekMobi-1

lm University Medical Center0 个研究点目标入组 21 人开始时间: 2021年4月8日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
21

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
N/a: Single Arm Study
盲法
Open (masking not used)

入排标准

年龄范围
18 Years 至 64 Years(—)
性别
All

入选标准

  • diagnosed cystic fibrosis

排除标准

  • - acute infection
  • - reduced general condition
  • - massive hemoptysis within the last 4 weeks
  • - pneumothorax within the last 6 weeks
  • - uncontrolled asthmatic symptoms
  • - unstable cardiovascular disease
  • - unstable pulmonary situation with dyspnea
  • - pregnancy

研究者

发起方
lm University Medical Center

相似试验

尚未招募
不适用
Clinical study ofacne mastitis
ITMCTR2200006068Shanghai Baoshan Hospital of Integrated Traditional Chinese and Western Medicine
已完成
不适用
Prospective, randomized, monocentric study for the determination of device-related dead spaces under controlled ventilation under general anesthesiaSpine operations in prone position
DRKS00015797St. Josef- und St. Elisabeth- Hospital gGmbH Klinik für Anästhesiologie und operative Intensivmedizin34
已完成
不适用
Prospective, randomized, monocentric study for the determination of device-related dead spaces in the MIRUS-System under controlled ventilation under general anesthesiaGeneral anaesthesia for orthopaedic surgeryJ80J44Adult respiratory distress syndromeOther chronic obstructive pulmonary disease
DRKS00021648Katholisches Klinikum gGmbH, Klinik für Anästhesiologie und operative Intensivmedizin40
尚未招募
Unknown
A prospective, single-center investigation of the safety and feasibility of a novel Microwave Ablation SystemC34C78.0Malignant neoplasm of bronchus and lungSecondary malignant neoplasm of lung
DRKS00032463Intuitive Surgical30
进行中(未招募)
1 期
Study to investigate the effect of riociguat on right heart size and function in pulmonary hypertensioSymptomatic pulmonary arterial hypertension with a mean pulmonary artery pressure >20 mmHg and pulmonary vascular resistance =2 Wood Units, pulmonary arterial wedge pressure =15 mmHg (Group I / Nice Clinical Classification of Pulmonary Hypertension (PH)) or CTEPH (Group IV) with hemodynamics as stated above defined as inoperable measured at least 3 months after start of full anticoagulation or with persisting or recurrent PH after pulmonary endarterectomy at least 6 months after surgeryMedDRA version: 20.0Level: HLTClassification code 10037401Term: Pulmonary hypertensionsSystem Organ Class: 100000004855
EUCTR2020-005462-34-DEThoraxklinik Heidelberg gGmbH30