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NCT04435353 Clinical Trial

Assessment of the Effectiveness of Vibroacoustic Therapy for Respiratory Failure Caused by COVID 19

Respiratory Distress Syndrome Clinical Trial

Official title:
Assessment of the Effectiveness of Vibroacoustic Therapy for Respiratory Failure Caused by COVID 19

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT04435353
Other study ID # AstanaMU
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date March 22, 2020
Est. completion date February 1, 2021

Study information
Verified date June 2020
Source Astana Medical University
Contact Irina Mukatova, PhD
Phone 8701 535 96 79
Email mukatovair@mail.ru
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Vibroacoustic pulmonary therapy in patients with COVID19 is believed to have a positive effect on oxygen status and a decrease in the duration of respiratory failure

Description:

This study aims to recruit the required number of patients for statistical identification of the effectiveness of vibroacoustic therapy in patients with COVID 19. Obligatory performance criteria will be presented by the duration of the course of respiratory failure and the duration of mechanical ventilation in the main and control groups. Optional performance criteria will be represented by oximetry values and standardization of laboratory parameters

Recruitment information / eligibility
Status Recruiting
Enrollment 200
Est. completion date February 1, 2021
Est. primary completion date December 31, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria:

1. adults

2. P/F less 300 torr

3. ARDS by Berlin convention

4. COVID 19 bilateral pneumonia

Exclusion Criteria:

1. children

2. acute brain stroke

3. acute coronary syndrome

4. pulmonary embolism

5. implanted pacemaker

Study Design

Related Conditions & MeSH terms

Intervention

Device:
• VibroLUNG
Lungs intensive therapy

Locations
Country Name City State
Kazakhstan Center of pulmonology Astana Astana
Kazakhstan Mukatova Irina Astana Nur-Sultan

Sponsors (1)
Lead Sponsor Collaborator
Astana Medical University

Country where clinical trial is conducted

Kazakhstan, 

Outcome
Type Measure Description Time frame Safety issue
Primary Recovery respiratory fail Regression of respiratory failure under the influence of vibroacoustic therapy 5-7 days
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