Recruitment

Recruitment Status
Completed

Inclusion Criteria

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

Exclusion Criteria

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

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

Exclusion Criteria

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

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