Longitudinal Assessment of Clinical Course and BIOmarkers in Severe Chronic AIRway Disease

NCT00555607 · Status: ACTIVE_NOT_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 233

Last updated 2021-03-03

No results posted yet for this study

Summary

The aim of the project is to study pathogenetic mechanisms in severe asthma and compare those mechanisms in chronic obstructive pulmonary disease (COPD) in order to test the hypothesis that severe asthma and COPD develop into similar chronic degenerative changes.

Conditions

Interventions

DRUG

prednisolone

Prednisolone oral tablets (10 mg active ingredient per tablet) once a day at a dose of 0.5mg/kg bodyweight, during 14 days.

Sponsors & Collaborators

  • University of Athens

    collaborator OTHER
  • University Hospital of Crete

    collaborator OTHER
  • Università degli Studi di Ferrara

    collaborator OTHER
  • University Ghent

    collaborator OTHER
  • Pulmonary Research Institute Grosshansdorf

    collaborator UNKNOWN
  • Leiden University Medical Center

    collaborator OTHER
  • Imperial College London

    collaborator OTHER
  • Université Montpellier

    collaborator OTHER
  • Fondazione C.N.R./Regione Toscana "G. Monasterio", Pisa, Italy

    collaborator OTHER_GOV
  • University of Southampton

    collaborator OTHER
  • Jagiellonian University

    collaborator OTHER
  • Karolinska Institutet

    lead OTHER

Principal Investigators

  • Sven-Erik Dahlén, Professor · Karolinska Institutet

Study Design

Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2002-03-31
Primary Completion
2005-04-30
Completion
2026-12-31

Countries

  • Sweden

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00555607 on ClinicalTrials.gov