ID
29666
Description
Study ID: 104385 Clinical Study ID: RES104385 Study Title: A randomised double-blind two-period crossover study to investigate the effect of treatment with repeat doses of a PPAR gamma agonist on the allergen-induced late asthmatic response in subjects with mild asthma compared with repeat doses of placebo Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00318630 https://clinicaltrials.gov/ct2/show/NCT00318630 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 1 Study Recruitment Status: Completed Generic Name: rosiglitazone Trade Name: Avandia XR,Avandia; Rosiglitazone XR,Avandia XR,Avandia Study Indication: Asthma This ODM-file contains Lung function testing: Exhaled nitric oxide, pulmonary function tests. Time: Treatment Period 1, Day 28.
Link
https://clinicaltrials.gov/ct2/show/NCT00318630
Keywords
Versions (1)
- 4/10/18 4/10/18 - Sarah Riepenhausen
Copyright Holder
GlaxoSmithKline
Uploaded on
April 10, 2018
DOI
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License
Creative Commons BY-NC 3.0
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GSK Influence of PPAR gamma agonist vs. Placebo on allergen-induced late asthmatic response NCT00318630
Lung function testing - Treatment Period 1, Day 28
- StudyEvent: ODM
Description
Pulmonary function tests / FEV 1
Alias
- UMLS CUI-1
- C0024119
- UMLS CUI-2
- C0429706
Description
Date of FEV1
Data type
date
Alias
- UMLS CUI [1,1]
- C0011008
- UMLS CUI [1,2]
- C0429706
Description
Time relative to Dosing.
Data type
text
Alias
- UMLS CUI [1,1]
- C0439564
- UMLS CUI [1,2]
- C0429706
Description
Hr : Min 00:00-23:59
Data type
time
Alias
- UMLS CUI [1,1]
- C0040223
- UMLS CUI [1,2]
- C0429706
Description
Reading 1 of FEV1
Data type
float
Measurement units
- L
Alias
- UMLS CUI [1,1]
- C0456984
- UMLS CUI [1,2]
- C0429706
Description
Reading 2 of FEV1
Data type
float
Measurement units
- L
Alias
- UMLS CUI [1,1]
- C0456984
- UMLS CUI [1,2]
- C0429706
Description
Reading 3 of FEV1
Data type
float
Measurement units
- L
Alias
- UMLS CUI [1,1]
- C0456984
- UMLS CUI [1,2]
- C0429706
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- StudyEvent: ODM
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