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

NCT ID: NCT03911947

Last Updated: 2021-01-14

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

113 participants

Study Classification

INTERVENTIONAL

Study Start Date

2019-05-02

Study Completion Date

2020-07-31

Brief Summary

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

Detailed Description

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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.

Conditions

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Respiratory Failure

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

PARALLEL

monitoring of treatment of patients with respiratory failure, the list of therapeutic measures which includes vibroacoustic therapy
Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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SaO2 (oxygen status)

Measurment 4 times per day, ABA (acid-bases analyses)

Group Type ACTIVE_COMPARATOR

Vibrolung

Intervention Type DEVICE

Device for vibroacoustic respiratory therapy

PaO2/FiO2 (respiratory index)

Measurment 4 times per day, ABA (acid-bases analyses)

Group Type ACTIVE_COMPARATOR

Vibrolung

Intervention Type DEVICE

Device for vibroacoustic respiratory therapy

AB (actual bicarbonat level)

Measurment 4 times per day, ABA (acid-bases analyses)

Group Type ACTIVE_COMPARATOR

Vibrolung

Intervention Type DEVICE

Device for vibroacoustic respiratory therapy

Interventions

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Vibrolung

Device for vibroacoustic respiratory therapy

Intervention Type DEVICE

Eligibility Criteria

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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
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Astana Medical University

OTHER

Sponsor Role lead

Responsible Party

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Aidos Konkayev

Chair of department

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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City clinical hospital №7

Almaty, , Kazakhstan

Site Status

City clinical hospital №1

Astana, , Kazakhstan

Site Status

National Cardiac Surgery Center

Astana, , Kazakhstan

Site Status

Scientific Research Institute of Traumatology and Orthopedics

Astana, , Kazakhstan

Site Status

Regional cardiology center

Shymkent, , Kazakhstan

Site Status

Countries

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Kazakhstan

Other Identifiers

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1972

Identifier Type: -

Identifier Source: org_study_id

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