Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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TERMINATED
NA
16 participants
INTERVENTIONAL
2005-06-30
2006-12-31
Brief Summary
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Detailed Description
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The COPD patients will not take prednisolone/placebo, but will either smoke 2 real or dummy cigarettes prior to scan. This protocol is similar to others used previously, which have proved acceptable to COPD patients and healthy smokers.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
DOUBLE
Interventions
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predisolone
Eligibility Criteria
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Inclusion Criteria
* FEV1\>80% predicted,
* no relevant medical or mental disorder, able to give informed consent and
* Patients with COPD,
* \>20 pack.year history,
* no other active lung disease,
* FEV1\<70%
* FEV1/VC\<70%,
* no other relevant medical or mental disorder, able to give informed consent
Exclusion Criteria
* ex-smokers
* other lung disorder
* relevant medical or mental illness
* recent (within 1 month) chest infection
* diabetes
50 Years
80 Years
ALL
No
Sponsors
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GlaxoSmithKline
INDUSTRY
Imperial College London
OTHER
Principal Investigators
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Hazel A Jones, PhD
Role: PRINCIPAL_INVESTIGATOR
Imperial College London
Locations
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Hammersmith Campus
London, , United Kingdom
Countries
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Other Identifiers
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FDG-PETsmoking
Identifier Type: -
Identifier Source: org_study_id
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