The Use of Vibrational Methods of Influencing the Lungs to Restore Their Functional State

  • STATUS
    Recruiting
  • End date
    Nov 22, 2023
  • participants needed
    240
  • sponsor
    Petrovsky National Research Centre of Surgery
Updated on 22 March 2022
Accepts healthy volunteers

Summary

There will be formed of groups for application of vibration methods on the lungs: the method of vibroacoustic lung massage using the "BARK VibroLUNG" device; the method of oscillating PEP therapy using Acapella DH Green; the method of hardware stimulation of cough with a mechanical insufflator-aspirator Comfort Cough Plus (Comfortable cough Plus). As a control group, classical manual chest massage with percussion and verbal stimulation of cough against the background of chest compressions with a total duration of 15 minutes will be used

Description

The patient signs an informed consent to participate in the study after 10-12 hours tracheal extubation and transfer of the patient to spontaneous respiration. The application of one or another method of influence is carried out by the method of random sampling (the envelope method). Next, a session is conducted using one of the methods of vibrational respiratory therapy. We are exploring the gas composition of arterial blood is examined, spirometry, and the respiratory rate is measured after 20 minutes of the procedure. Further, respiratory therapy sessions are repeated 3 times a day for three days

Details
Condition Respiratory Failure
Treatment prevention of respiratory failure
Clinical Study IdentifierNCT05159401
SponsorPetrovsky National Research Centre of Surgery
Last Modified on22 March 2022

Eligibility

Yes No Not Sure

Inclusion Criteria

Age from 18 years to 80 years inclusive
Performed cardiac surgery in IC conditions
The patient's consent to participate in this study

Exclusion Criteria

Lack of productive contact with the patient
Any disorder in the central nervous system in the perioperative period (acute cerebrovascular accident, coma, posthypoxic encephalopathy), being on a ventilator
Unstable hemodynamics or hemodynamically significant rhythm disturbances
Shocks of various etiologies
Inability to provide respiratory protection, high risk of aspiration
Refusal of the patient to participate in this study
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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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