Recruitment

Recruitment Status
Completed

Inclusion Criterias

Patients ≤24h after tracheostomy and regular patient's consent
Patients ≤24h after tracheostomy and regular patient's consent

Exclusion Criterias

Patients with acute or imminent sepsis
No regular patient's consent
Patients >24h after tracheostomy
...
Patients with acute or imminent sepsis
No regular patient's consent
Patients >24h after tracheostomy
Patients with poorly adjusted pulmonary disease
Patients with immunosuppressive therapy
Known allergy for ingredients
Patients with chronic respiratory insufficiency
Patients with existing bronchopulmonary inflammation

Summary

Conditions
Other Tracheostomy Complication
Type
Interventional
Design
  • Allocation: Randomized
  • Intervention Model: Parallel Assignment
  • Masking: Double (Participant, Investigator)
  • Primary Purpose: Supportive Care

Participation Requirements

Age
Younger than 125 years
Gender
Both males and females

Inclusion Criterias

Patients ≤24h after tracheostomy and regular patient's consent
Patients ≤24h after tracheostomy and regular patient's consent

Exclusion Criterias

Patients with acute or imminent sepsis
No regular patient's consent
Patients >24h after tracheostomy
...
Patients with acute or imminent sepsis
No regular patient's consent
Patients >24h after tracheostomy
Patients with poorly adjusted pulmonary disease
Patients with immunosuppressive therapy
Known allergy for ingredients
Patients with chronic respiratory insufficiency
Patients with existing bronchopulmonary inflammation

Locations

Munich, Bavaria, 81675
Munich, Bavaria, 81675

Tracking Information

NCT #
NCT02157129
Collaborators
Not Provided
Investigators
  • Principal Investigator: Andreas Knopf, PD Dr. HNO, Klinikum rechts der Isar, TU München
  • Andreas Knopf, PD Dr. HNO, Klinikum rechts der Isar, TU München