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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02743624
Other study ID # tematicomusculoUTI
Secondary ID
Status Completed
Phase N/A
First received March 18, 2016
Last updated January 18, 2017
Start date February 2016
Est. completion date December 2016

Study information

Verified date August 2016
Source University of Sao Paulo General Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The indications for mechanical ventilation (MV) include excessive work of breathing, with or without evidence of respiratory muscle fatigue. The setting of the MV is still a challenge because it is based on criteria understudied, often subjective and observer-dependent. Despite several studies, to our knowledge has never been done before is the precise definition of the optimal range of ventilatory support. Novel and recognizable diagnostic techniques will be applied. No single parameter of the breathing pattern has good accuracy for the adjustment of ventilatory support. Non-invasive measures such as P0.1 and rate of muscle relaxation may have good accuracy for the adjustment of ventilatory support.


Description:

Use of excessive pressure support


Recruitment information / eligibility

Status Completed
Enrollment 27
Est. completion date December 2016
Est. primary completion date November 2016
Accepts healthy volunteers No
Gender All
Age group 18 Years to 90 Years
Eligibility Inclusion Criteria:

- patients under invasive mechanical ventilation for 48h

- patients without the objective of complete rest of the respiratory muscles. This decision will be on the discretion of the attending physician,

- spontaneous breathing,

- clinically stability.

Exclusion Criteria:

- Previous disease of the central nervous system that can lead to respiratory changes.

- Previous disease of the peripheral nervous system that can lead to respiratory changes

- Previous muscular disease.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Variation of the level of pressure support during the mechanical ventilation
The pressure support of the patient was changed form the baseline to 20 cmH20 and then stepwise decreased to 2 cmH20,

Locations

Country Name City State
Brazil Hearth Institute - University of Sao Paulo Sao Paulo SP
Brazil Hospital Clinicas Sao Paulo Sao Paulo

Sponsors (1)

Lead Sponsor Collaborator
University of Sao Paulo General Hospital

Country where clinical trial is conducted

Brazil, 

Outcome

Type Measure Description Time frame Safety issue
Primary Measuring muscular force Muscular force measured by inspiratory force in centimeters of water (cmH2O) From the baseline ventilation to the minimum level of pressure support. Around 3 hours
Secondary Measuring inspiratory drive Inspiratory drive measured in cmH2O in the first 100 milliseconds of the inspiration From the baseline ventilation to the minimum level of pressure support. Around 3 hours
Secondary Measuring endurance Endurance measured by the maximal relaxation rate (cmH2O/10ms) From the baseline ventilation to the minimum level of pressure support. Around 3 hours
See also
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