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

P

Petrovsky National Research Centre of Surgery

Status

Completed

Conditions

Respiratory Failure

Treatments

Procedure: prevention of respiratory failure

Study type

Interventional

Funder types

Other

Identifiers

NCT05159401
09052021

Details and patient eligibility

About

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

Full 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

Enrollment

240 patients

Sex

All

Ages

18 to 80 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

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

Exclusion criteria

  1. Lack of productive contact with the patient
  2. Any disorder in the central nervous system in the perioperative period (acute cerebrovascular accident, coma, posthypoxic encephalopathy), being on a ventilator.
  3. Unstable hemodynamics or hemodynamically significant rhythm disturbances
  4. Shocks of various etiologies
  5. Inability to provide respiratory protection, high risk of aspiration
  6. Refusal of the patient to participate in this study

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Factorial Assignment

Masking

None (Open label)

240 participants in 4 patient groups

the first group: the method of vibroacoustic lung massage using the "BARK VibroLUNG" device
Experimental group
Description:
dynamics blood saturation by pulse oximeter,minute inspiratory lung volume befor/after research
Treatment:
Procedure: prevention of respiratory failure
the second group:the method of oscillating REР therapy using Acapella DH Green
Experimental group
Description:
dynamics blood saturation by pulse oximeter,minute inspiratory lung volume befor/after research
Treatment:
Procedure: prevention of respiratory failure
the third group:the method of hardware stimulation of cough (Comfortable cough Plus)
Experimental group
Description:
dynamics blood saturation by pulse oximeter,minute inspiratory lung volume befor/after research
Treatment:
Procedure: prevention of respiratory failure
the fourth group:classical manual chest massage with percussion
Experimental group
Description:
dynamics blood saturation by pulse oximeter,minute inspiratory lung volume befor/after research
Treatment:
Procedure: prevention of respiratory failure

Trial contacts and locations

1

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Central trial contact

Alexander А. Eremenko, prof; Darya V. Ryabova

Data sourced from clinicaltrials.gov

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