Recruitment

Recruitment Status
Active, not recruiting
Estimated Enrollment
10

Summary

Conditions
Respiratory Distress Syndrome
Type
Interventional
Phase
Not Applicable
Design
Allocation: N/AIntervention Model: Single Group AssignmentIntervention Model Description: intervention of a device product being evaluated in a small clinical trial to determine the feasibility of the productMasking: None (Open Label)Primary Purpose: Device Feasibility

Participation Requirements

Age
Younger than 3036 years
Gender
Both males and females

Description

A prospective study to assess the safety and efficacy of surfactant administration via thin catheter using a specially adapted VNscope, originally used for endotracheal intubation and adapted for the administration of surfactant without the placement of an endotracheal tube. Once neonates present re...

A prospective study to assess the safety and efficacy of surfactant administration via thin catheter using a specially adapted VNscope, originally used for endotracheal intubation and adapted for the administration of surfactant without the placement of an endotracheal tube. Once neonates present respiratory distress, the adapted scope will be used - clinical and outcome measures will be collected to asses the safety and efficacy of the use

Tracking Information

NCT #
NCT03846960
Collaborators
Carmel Medical Center
Investigators
Principal Investigator: Gil talmon, dr haemek medical center