Skip to content

Switching From Tobramycin Inhalation Treatment to Tobramycin Inhaler Treatment: The Effect on CF Patients' Adherence and Quality of Life

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01749644
Enrollment
40
Registered
2012-12-17
Start date
2013-01-31
Completion date
2015-01-31
Last updated
2012-12-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Alteration in Quality of Life of CF Patients, Following Change of Treatment From Antibiotic Inhalation to Antibiotic Inhaler

Keywords

Cystic Fibrosis, Chronic Pseudomonas Infection, Inhaled Tobramycin

Brief summary

Pseudomonas is a common and virulent respiratory bacteria in patients with Cystic Fibrosis (CF). With time, the infection with Pseudomonas becomes chronic and very difficult to eradicate. The standard treatment of chronic Pseudomonas infection is inhaled Tobramycin which is given every other month.. Inhalation of Tobramycin was proven as an effective treatment that improves the respiratory function and reduces the concentration of bacteria in the sputum. However, inhaled treatment lasts between 15 to 30 minutes twice a day and therefore adherence is a major problem. The effect of switching from inhalation treatment to inhaler treatment on patient's adherence and quality of life has not been studied.

Interventions

None listed

Sponsors

Sheba Medical Center
Lead SponsorOTHER_GOV

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
6 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age 6 years and above, Chronic Pseudomonas infection

Exclusion criteria

* Younger than 6 years; No chronic PSeudomonas infection

Design outcomes

Primary

MeasureTime frame
Improvement in quality of life1 year

Secondary

MeasureTime frameDescription
Difference in exacerbation events1 yearTo be measured by: Worsening of CF symptoms such as coughing, sputum, deterioration in FEV1, all of which require hospitalization

Countries

Israel

Contacts

Primary ContactOri Sarouk, MD
ifat.sarouk@sheba.health.gov.il97235302884

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026