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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00421018
Other study ID # 20050166
Secondary ID
Status Completed
Phase N/A
First received January 10, 2007
Last updated August 14, 2012
Start date November 2006
Est. completion date April 2010

Study information

Verified date August 2012
Source Karolinska Institutet
Contact n/a
Is FDA regulated No
Health authority Sweden: The Ministry of Education and Cultural Affairs
Study type Interventional

Clinical Trial Summary

The purpose of this study is to determine whether use of exhaled NO (nitric oxide) to regulate the anti-inflammatory treatment leads to increased asthma-related quality of life in patients with allergic asthma


Recruitment information / eligibility

Status Completed
Enrollment 187
Est. completion date April 2010
Est. primary completion date April 2010
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 64 Years
Eligibility Inclusion Criteria:

- Age 18-64

- Clinical diagnosis of Asthma

- Glucocorticoid treatment > 6 months.

- Verified Allergy

- Read and speak Swedish

Exclusion Criteria:

- Smoking

- Current regular treatment with long-acting beta2-agonist

- Treatment with Singulair only or in combination with glucocorticoids

- Taking part in other research study

- Pregnancy or breast-feeding

- Unstable Asthma

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Drug:
Single corticosteroid inhalers and Singulair
Treatment steps according to preset algorithm

Locations

Country Name City State
Sweden Runby Primary Health Care Center Upplands Väsby

Sponsors (9)

Lead Sponsor Collaborator
Karolinska Institutet Aerocrine AB, Meda AB, Merck Sharp & Dohme Corp., Phadia AB, Stockholm County Council, Sweden, Swedish Council for Working Life and Social Research, The Swedish Research Council, Uppsala University

Country where clinical trial is conducted

Sweden, 

Outcome

Type Measure Description Time frame Safety issue
Primary Mini-AQLQ (Asthma-Related Quality of Life) 1 year No
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