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NCT03911947 Clinical Trial

Evaluation of the Effectiveness of Vibroacoustic Therapy in the Complex Treatment of Acute Respiratory Failure

Respiratory Failure Clinical Trial

Official title:
Assessing the Ventilatory Parameters in Patients With Acute Respiratory Failure After Vibroacoustic Pulmonary Therapy.

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03911947
Other study ID # 1972
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date May 2, 2019
Est. completion date July 31, 2020

Study information
Verified date January 2021
Source Astana Medical University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Evaluation of the effectiveness of vibroacoustic therapy in the complex treatment of acute respiratory failure

Description:

Assessing the dynamics of changes in physical, instrumental and laboratory parameters in patients with acute respiratory failure taken in the study according to the inclusion criteria and comparing the results with the control group, studying the effectiveness of vibroacoustic lung therapy.

Recruitment information / eligibility
Status Completed
Enrollment 113
Est. completion date July 31, 2020
Est. primary completion date April 30, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - adults - P/F less 300 torr - ARDS by Berlin convention Exclusion Criteria: - children - acute stroke - acute coronary syndrome - DVT - implanted pacemaker - rib fracture - infection on chest

Study Design

Related Conditions & MeSH terms

Intervention

Device:
• Vibrolung
Device for vibroacoustic respiratory therapy

Locations
Country Name City State
Kazakhstan City clinical hospital ?7 Almaty
Kazakhstan City clinical hospital ?1 Astana
Kazakhstan National Cardiac Surgery Center Astana
Kazakhstan Scientific Research Institute of Traumatology and Orthopedics Astana
Kazakhstan Regional cardiology center Shymkent

Sponsors (1)
Lead Sponsor Collaborator
Astana Medical University

Country where clinical trial is conducted

Kazakhstan, 

Outcome
Type Measure Description Time frame Safety issue
Primary Change of time spent on ventilation Changing of the time spent by patients on mechanical ventilation 1-2 days
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