Examination of Cardiovascular Function/ Cardio Respiratory Interaction on Spontaneous Breathing Trials in Patients in the Prolonged Weaning
NCT ID: NCT02569385
Last Updated: 2015-10-06
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
20 participants
OBSERVATIONAL
2015-08-31
2016-08-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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CASE_ONLY
PROSPECTIVE
Study Groups
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spontaneous breathing trials
spontaneous breathing trials in patients with prolonged weaning
Spontaneous breathing trial
Interventions
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Spontaneous breathing trial
Eligibility Criteria
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Inclusion Criteria
* written informed consent Prior to study participation
* patient in prolonged weaning with NYHA I-II and an actual positive Ventilator Screening test:
1. PaO2 ≥ 60 mmHg at FiO2 ≤ 0.4
2. PEEP ≤ 8 cmH2O
3. Glasgow Coma Scale \> 13
4. Temp. \< 38°C
5. Hb \> 80-100 g/L
6. less requirement on catecholamines (\<0.1µg/kg/min)
* and on these patients are already performed a spontaneous breathing trial with following result:
1. abortion this spontaneous breathing trial \< 30min, but possible \> 10min
2. reason for an abortion was NOT hypercapnia
Exclusion Criteria
* patient with heart failure (NYHA III-IV) and/ or other cardiac comorbidity
* acute NSTEMI (non-ST-segment elevation myocardial infarction)
* pregnancy and breast-feeding
18 Years
ALL
Yes
Sponsors
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RWTH Aachen University
OTHER
Responsible Party
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Principal Investigators
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Michael Dreher, MD
Role: PRINCIPAL_INVESTIGATOR
Uniklinik RWTH Aachen, Med. Klinik I
Locations
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University Hospital RWTH Aachen, Department of Medical Clinic I
Aachen, , Germany
Countries
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Central Contacts
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Other Identifiers
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CTC-A 15-034
Identifier Type: -
Identifier Source: org_study_id
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