Skip to main content
Clinical Trials/NCT02569385
NCT02569385
Unknown
N/A

Examination of Cardiovascular Function/ Cardio Respiratory Interaction on Spontaneous Breathing Trials in Patients in the Prolonged Weaning

RWTH Aachen University1 site in 1 country20 target enrollmentAugust 2015

Overview

Phase
N/A
Intervention
Not specified
Conditions
Cardiovascular Disease
Sponsor
RWTH Aachen University
Enrollment
20
Locations
1
Primary Endpoint
Baseline measurement (Modus "CPAP-PS") in patient with prolonged weaning
Last Updated
10 years ago

Overview

Brief Summary

The aim of the present study is to determine the cardiovascular function/ cardio respiratory interaction on spontaneous breathing trials in patients with prolonged weaning.

Registry
clinicaltrials.gov
Start Date
August 2015
End Date
August 2016
Last Updated
10 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • legal Age (≥18 years)
  • written informed consent Prior to study participation
  • patient in prolonged weaning with NYHA I-II and an actual positive Ventilator Screening test:
  • PaO2 ≥ 60 mmHg at FiO2 ≤ 0.4
  • PEEP ≤ 8 cmH2O
  • Glasgow Coma Scale \> 13
  • Temp. \< 38°C
  • Hb \> 80-100 g/L
  • less requirement on catecholamines (\<0.1µg/kg/min)
  • and on these patients are already performed a spontaneous breathing trial with following result:

Exclusion Criteria

  • weaning patients are assigned on Group 1-2
  • patient with heart failure (NYHA III-IV) and/ or other cardiac comorbidity
  • acute NSTEMI (non-ST-segment elevation myocardial infarction)
  • pregnancy and breast-feeding

Outcomes

Primary Outcomes

Baseline measurement (Modus "CPAP-PS") in patient with prolonged weaning

Time Frame: 12 months

under pressure support Ventilation are determined some measurement (e.g. breathing rate)

Secondary Outcomes

  • Intervention measurement in patient with prolonged weaning(12 months)

Study Sites (1)

Loading locations...

Similar Trials