Status:
COMPLETED
A Long Term Prospective Follow Up Study For The CATO Study (SAS30018/SER9702)
Lead Sponsor:
GlaxoSmithKline
Conditions:
Asthma
Eligibility:
All Genders
Brief Summary
The CATO population is a very well documented population during two years. During this study patients were treated according to the CATO algorithm, after that patient were treated according to the Dut...
Detailed Description
A long term follow up study for a comparison of stepwise treatment of asthmatic children with Salmeterol/Fluticasone propionate combination product (Seretide®) and/or Fluticasone propionate (Flixotide...
Eligibility Criteria
Inclusion
- Inclusion criteria:
- Any subject who has given informed consent to participate in the CATO study, and has met all the criteria required for randomisation into the clinical study may take part in this follow up study
- Under the age of 18 years Subjects and both parent(s)/guardian(s) who have given written informed consent to participate in the study
- Subjects from 18 years and older who have given written informed consent to participate in the study
- Exclusion criteria:
- Experienced an acute asthma exacerbation requiring emergency room treatment within 4 weeks or hospitalisation within 4 weeks of visit 1
- Any use of oral/parenteral or depot corticosteroid within 4 weeks of visit 1
- Subjects who are pregnant (a pregnancy test can be performed at the investigator's discretion)
Exclusion
Key Trial Info
Start Date :
January 1 2007
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
October 1 2007
Estimated Enrollment :
137 Patients enrolled
Trial Details
Trial ID
NCT00441675
Start Date
January 1 2007
End Date
October 1 2007
Last Update
March 19 2012
Active Locations (15)
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1
GSK Investigational Site
Alkmaar, Netherlands, 1815 JD
2
GSK Investigational Site
Almere Stad, Netherlands, 1315 RA
3
GSK Investigational Site
Amsterdam, Netherlands, 1081 HV
4
GSK Investigational Site
Amsterdam, Netherlands, 1105 AZ