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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT02281695
Other study ID # MHO 001
Secondary ID
Status Withdrawn
Phase N/A
First received
Last updated
Start date October 2014
Est. completion date December 2018

Study information

Verified date August 2022
Source Marienhospital Osnabrück
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to determine the differences in oxygenation and decarboxylation between two weaning processes.


Description:

First, during controlled mechanical ventilation all patients will be ventilated for 5 minutes with 100% oxygen. After 5 minutes an PaO2/FiO2 will be calculated and compared with a PaO2/FiO2 during ventilation with FiO2 - 30%. The patients will be divided in two sections: Section A are the patients with less than 24 hours mechanical ventilation until weaning start. Section B are the patients with more than 24 hours until weaning start. The patients in every section will be further divided in two groups. Group 1 will be weaned starting with a PEEP equal with P mean during BiPAP, Group 2 will be weaned starting with a PEEP equal with PEEP during BiPAP. Further, the weaning will be conducted after an known algorithm. The differences in the oxygenation and decarboxylation will be measured after 30 and 120 Minutes for Group A and after 30, 120, 240, 360 Minutes for Group B.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date December 2018
Est. primary completion date November 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - All Patients that are mechanical ventilated on the intensive care unit. Exclusion Criteria: - Patients under 18 years of age - Patients that where in an other study in the last 30 days - Patients that are enrolled in other studies - Pregnant woman - Nursing mothers - Existing severe Lung disease - Existing COPD Gold IV

Study Design


Related Conditions & MeSH terms


Intervention

Other:
PEEP adjusment during the Weaning process
The PEEP will be adjusted after an previously established algorithm and the differences in the arterial blood oxygen partial pressure will be compared.

Locations

Country Name City State
Germany Marienhospital Osnabrück Osnabrück Niedersachsen

Sponsors (1)

Lead Sponsor Collaborator
Marienhospital Osnabrück

Country where clinical trial is conducted

Germany, 

Outcome

Type Measure Description Time frame Safety issue
Primary Changes in the Oxygen Partial Pressure and CO2 Partial Pressure in the arterial blood gas analysis 30, 60, 90, 120, 360 Minutes
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