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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT01749644
Other study ID # SHEBA-12-9640-OE-CTIL
Secondary ID
Status Not yet recruiting
Phase N/A
First received December 12, 2012
Last updated December 15, 2012
Start date January 2013
Est. completion date January 2015

Study information

Verified date December 2012
Source Sheba Medical Center
Contact Ori Sarouk, MD
Phone 97235302884
Email ifat.sarouk@sheba.health.gov.il
Is FDA regulated No
Health authority Israel: Ministry of Health
Study type Observational

Clinical Trial 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.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 40
Est. completion date January 2015
Est. primary completion date June 2014
Accepts healthy volunteers No
Gender Both
Age group 6 Years and older
Eligibility Inclusion Criteria:

- Age 6 years and above, Chronic Pseudomonas infection

Exclusion Criteria:

- Younger than 6 years; No chronic PSeudomonas infection

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms

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

Locations

Country Name City State
Israel Safra Children's Hospital, Sheba Medical Center Ramat Gan

Sponsors (1)

Lead Sponsor Collaborator
Sheba Medical Center

Country where clinical trial is conducted

Israel, 

Outcome

Type Measure Description Time frame Safety issue
Primary Improvement in quality of life 1 year No
Secondary Difference in exacerbation events To be measured by:
Worsening of CF symptoms such as coughing, sputum, deterioration in FEV1, all of which require hospitalization
1 year No