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Modified Rescue High Frequency Oscillatory Ventilation Protocol Improves Outcome in Pediatric Patients with Severe Acute:Respiratory Distress Syndrome: A randomized control trial - Trial PACTR202210850139462

Access comprehensive clinical trial information for PACTR202210850139462 through Pure Global AI's free database. This Phase 4 trial is sponsored by Faculty of medicine of tanta university and is currently Recruiting. The study focuses on Respiratory; Paediatrics.

This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to Pan Africa Clinical Trials Registry data, helping medical device and pharmaceutical companies navigate clinical research efficiently.

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PACTR202210850139462
Phase 4
Recruiting
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Trial Details
Pan Africa Clinical Trials Registry โ€ข PACTR202210850139462
Pure Global
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Modified Rescue High Frequency Oscillatory Ventilation Protocol Improves Outcome in Pediatric Patients with Severe Acute:Respiratory Distress Syndrome: A randomized control trial
Modified Rescue High Frequency Oscillatory Ventilation Protocol Improves Outcome in Pediatric Patients with Severe Acute Respiratory Distress Syndrome

Study Focus

Respiratory; Paediatrics

device

Sponsor & Location

Faculty of medicine of tanta university

Doaa El Amrousy

Egypt

Timeline & Enrollment

Phase 4

Jan 01, 1900

Jan 01, 1900

Summary

High frequency oscillatory ventilation (HFOV) is used mainly as a rescue mode in pediatric acute respiratory distress syndrome (PARDS). Although it may improve oxygenation, its overall benefit is still controversial. We aimed to compare a modified protocol of rescue introduction of HFOV and early weaning to conventional mechanical ventilation (CMV) with CMV in PARDS.

ICD-10 Classifications

Other postprocedural respiratory disorders
Respiratory disorder, unspecified
Other specified respiratory disorders
Diseases of the respiratory system
Other respiratory disorders

Data Source

Pan Africa Clinical Trials Registry

PACTR202210850139462

Device Trial