Actively Recruiting
The Course of Acute Respiratory Failure in Geriatric Patients With Hip Fracture Using Different Modes of a Vibroacoustic Device for the Lungs
Led by Astana Medical University · Updated on 2026-04-08
60
Participants Needed
1
Research Sites
143 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
A medical professional trained in the procedure and use of the device will conduct the vibroacoustic therapy session. He will also take blood samples. In the control group, patients will undergo vibroacoustic pulmonary therapy in the "Pneumonia" mode, and in the control group, in the "Prevention" mode. Vibroacoustic pulmonary therapy will be conducted over a period of 5 days. A similar algorithm of actions is planned for both groups. VALT sessions will be conducted 4-6 times a day for 5 minutes in combination with treatment according to the protocol for the use of "Vibroacoustic Therapy" of the lungs of the Ministry of Health of the Republic of Kazakhstan. The device's emitters will be applied to the affected areas of the lungs. Since the device has long cords for the emitters and is portable, it is not difficult to change the patient's position and does not require their active participation, which is important for patients on ventilators and with limited mobility.
CONDITIONS
Official Title
The Course of Acute Respiratory Failure in Geriatric Patients With Hip Fracture Using Different Modes of a Vibroacoustic Device for the Lungs
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Respiratory failure
- Hip fracture
- Injury Severity Score no higher than 8 points
- Age between 60 and 85 years
You will not qualify if you...
- All contraindications for the use of the device
- Terminal condition
- Shock
- Paradoxical pathological breathing
- Hypertensive crisis
- Severe hypocoagulation with risk of bleeding
- Severe hypercoagulation with risk of thrombus or embolus migration
- Acute cerebrovascular accident within 1-3 days
- Brain edema
- Multiple purulent or burn wounds in the treatment area
- Unstable rib fractures
- Pneumomediastinum or subcutaneous emphysema of the chest
- Osteomyelitis of ribs or thoracic spine
- Spinal fracture without orthopedic fixation
- Chest or abdominal trauma with bleeding
- Injury Severity Score greater than 8 points
- Decompensated concomitant diseases
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Astana medical university
Astana, Kazakhstan, 010000
Actively Recruiting
Research Team
A
Assema Bekniyazova
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
BASIC_SCIENCE
Number of Arms
2
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