- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05143372
Influence of Vibroacoustic Therapy Modes on the Course of Coronavirus Infection
February 9, 2024 updated by: Aidos Konkayev, Astana Medical University
The Effect of Various Modes of Vibroacoustic Therapy on the Course of Coronavirus Infection Complicated by Acute Respiratory Failure.
Assessment of the dynamics of changes in physical, instrumental and laboratory parameters in patients with identified coronavirus infection complicated by acute respiratory failure included in the study in accordance with the inclusion criteria, and comparison of the results with the control group, study of the effect of modes when using vibroacoustic lung therapy.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
60
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Astana, Kazakhstan, 010000
- NATIONAL CENTER Scientific Center of Traumatology and Orthopedics named after Academician Batpenov N.D.
-
Astana, Kazakhstan
- Multidisciplinary city hospital No. 3 of Nursultan
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Astana, Kazakhstan
- Multidisciplinary Infectious Diseases Hospital of Nursultan
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- adults
- P/F less 300 torr
- COVID-19 Virus Infection
Exclusion Criteria:
- children
- acute stroke
- acute coronary syndrome
- DVT
- implanted pacemaker
- rib fracture
- infection on chest
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: SaO2 (oxygen status)
Measurment 4 times per day, ABA (acid-bases analyses)
|
Vibroacoustic respiratory therapy
|
|
Active Comparator: PaO2/FiO2 (respiratory index)
Measurment 4 times per day, ABA (acid-bases analyses)
|
Vibroacoustic respiratory therapy
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change of time spent on ventilation
Time Frame: 1-2 days
|
Changing of the time spent by patients on mechanical ventilation
|
1-2 days
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
November 9, 2021
Primary Completion (Actual)
September 30, 2023
Study Completion (Actual)
September 30, 2023
Study Registration Dates
First Submitted
November 22, 2021
First Submitted That Met QC Criteria
November 22, 2021
First Posted (Actual)
December 3, 2021
Study Record Updates
Last Update Posted (Actual)
February 12, 2024
Last Update Submitted That Met QC Criteria
February 9, 2024
Last Verified
February 1, 2024
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Coronaviridae Infections
- Nidovirales Infections
- RNA Virus Infections
- Virus Diseases
- Infections
- Respiratory Tract Infections
- Respiratory Tract Diseases
- Respiration Disorders
- Pneumonia, Viral
- Pneumonia
- Lung Diseases
- COVID-19
- Coronavirus Infections
- Respiratory Insufficiency
- Respiratory Distress Syndrome
Other Study ID Numbers
- СТЛ-000215
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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