ID
29677
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 Screening Part 4 - ECG and Pulmonary function parts Exhaled nitric oxide and AMP Challenge.
Link
https://clinicaltrials.gov/ct2/show/NCT00318630
Keywords
Versions (2)
- 4/10/18 4/10/18 - Sarah Riepenhausen
- 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
Screening Part 4 - ECG and Pulmonary function (exhaled nitric oxide and AMP Challenge)
Description
Exhaled nitric oxide
Alias
- UMLS CUI-1
- C3700245
Description
Exhaled nitric oxide - Date
Data type
date
Alias
- UMLS CUI [1,1]
- C3700245
- UMLS CUI [1,2]
- C0011008
Description
Planned relative time
Data type
text
Alias
- UMLS CUI [1,1]
- C0439564
- UMLS CUI [1,2]
- C3700245
Description
Actual Time of First Reading
Data type
time
Alias
- UMLS CUI [1,1]
- C3700245
- UMLS CUI [1,2]
- C0040223
Description
Reading 1
Data type
float
Measurement units
- ppb
Alias
- UMLS CUI [1,1]
- C3700245
- UMLS CUI [1,2]
- C0456984
Description
Reading 2
Data type
float
Measurement units
- ppb
Alias
- UMLS CUI [1,1]
- C3700245
- UMLS CUI [1,2]
- C0456984
Description
Reading 3
Data type
float
Measurement units
- ppb
Alias
- UMLS CUI [1,1]
- C3700245
- UMLS CUI [1,2]
- C0456984
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]
- C0748133
Description
Pulmonary Function Time
Data type
time
Alias
- UMLS CUI [1,1]
- C0040223
- UMLS CUI [1,2]
- C0024119
Description
FEV1 Reading 1
Data type
float
Measurement units
- L
Alias
- UMLS CUI [1,1]
- C0456984
- UMLS CUI [1,2]
- C0429706
Description
FEV1 Reading 2
Data type
float
Measurement units
- L
Alias
- UMLS CUI [1,1]
- C0456984
- UMLS CUI [1,2]
- C0429706
Description
FEV1 Reading 3
Data type
float
Measurement units
- L
Alias
- UMLS CUI [1,1]
- C0456984
- UMLS CUI [1,2]
- C0429706
Description
Value A in investigator Calculation
Data type
float
Measurement units
- L
Alias
- UMLS CUI [1,1]
- C0456984
- UMLS CUI [1,2]
- C0429706
Description
Value B in Investigator Calculation
Data type
float
Measurement units
- L
Alias
- UMLS CUI [1,1]
- C0748133
- UMLS CUI [1,2]
- C0086715
Description
Investigator Calculation: A / B x 100 FEV1 must be > 70% of predicted at Screening.
Data type
float
Measurement units
- %
Alias
- UMLS CUI [1]
- C0730561
Description
Pulmonary function tests: Pre-AMP Challenge
Alias
- UMLS CUI-1
- C0024119
- UMLS CUI-2
- C1096479
- UMLS CUI-3
- C3812758
Description
pre-AMP pulmonary function test date
Data type
date
Alias
- UMLS CUI [1,1]
- C0011008
- UMLS CUI [1,2]
- C0024119
- UMLS CUI [1,3]
- C1096479
- UMLS CUI [1,4]
- C3812758
Description
Time relative to start of challenge. 3 pre-saline measurements are required.
Data type
text
Alias
- UMLS CUI [1,1]
- C0439564
- UMLS CUI [1,2]
- C0748133
Description
Time of FEV1
Data type
time
Alias
- UMLS CUI [1,1]
- C0040223
- UMLS CUI [1,2]
- C0429706
Description
FEV1 Reading
Data type
float
Measurement units
- L
Alias
- UMLS CUI [1,1]
- C0456984
- UMLS CUI [1,2]
- C0429706
Description
Pulmonary function tests: AMP Challenge
Alias
- UMLS CUI-1
- C0024119
- UMLS CUI-2
- C1096479
Description
AMP-Challenge Date
Data type
date
Alias
- UMLS CUI [1,1]
- C0011008
- UMLS CUI [1,2]
- C1096479
Description
Inhaled Substance
Data type
text
Alias
- UMLS CUI [1,1]
- C0205535
- UMLS CUI [1,2]
- C0001465
- UMLS CUI [2,1]
- C0205535
- UMLS CUI [2,2]
- C0036082
Description
Following the baseline assessment in which FEV1 is measured after inhalation of saline, subjects are to inhale doubling increments of AMP until a ≥20percent fall in FEV1 from the baseline saline value is achieved. 0.000 is the concentration value for saline.
Data type
text
Measurement units
- mg/mL
Alias
- UMLS CUI [1,1]
- C1446561
- UMLS CUI [1,2]
- C0001465
Description
Use this item, if historical concentrations instead of the concentrations given in the item "challenge concentration (New Subjects)" are used. Following the baseline assessment in which FEV1 is measured after inhalation of saline, subjects are to inhale doubling increments of AMP until a ≥20percent fall in FEV1 from the baseline saline value is achieved. Use 0.000 for saline inhaltation.
Data type
float
Measurement units
- mg/mL
Alias
- UMLS CUI [1,1]
- C1446561
- UMLS CUI [1,2]
- C0001465
Description
Fill in only for saline inhalation.
Data type
time
Alias
- UMLS CUI [1,1]
- C1301880
- UMLS CUI [1,2]
- C0001559
Description
Stop Time of Inhalation
Data type
time
Alias
- UMLS CUI [1,1]
- C1522314
- UMLS CUI [1,2]
- C0001559
Description
Both timepoints must be filled after each inhalation. Time relative to stop time of inhalation.
Data type
text
Alias
- UMLS CUI [1,1]
- C0439564
- UMLS CUI [1,2]
- C0205535
- UMLS CUI [1,3]
- C0748133
Description
Pulmonary function time
Data type
time
Alias
- UMLS CUI [1,1]
- C0040223
- UMLS CUI [1,2]
- C0429706
Description
FEV1 Result
Data type
float
Measurement units
- L
Alias
- UMLS CUI [1,1]
- C0429706
- UMLS CUI [1,2]
- C1096479
Description
Pulmonary function tests: Post-AMP Challenge
Alias
- UMLS CUI-1
- C0231921
- UMLS CUI-2
- C1096479
- UMLS CUI-3
- C0439568
Description
Date of post-challenge FEV1
Data type
date
Alias
- UMLS CUI [1,1]
- C0011008
- UMLS CUI [1,2]
- C0429706
- UMLS CUI [1,3]
- C0439568
Description
Time relative to end of challenge: Post-challenge 6 measurements are required.
Data type
time
Alias
- UMLS CUI [1,1]
- C0040223
- UMLS CUI [1,2]
- C0429706
- UMLS CUI [1,3]
- C0439568
Description
Record use of rescue Salbutamol on the Concomitant Medications page.
Data type
float
Measurement units
- L
Alias
- UMLS CUI [1,1]
- C0429706
- UMLS CUI [1,2]
- C1274040
- UMLS CUI [1,3]
- C0439568
Description
PC20 (AMP Challenge)
Alias
- UMLS CUI-1
- C1446561
- UMLS CUI-2
- C0001465
- UMLS CUI-3
- C0429706
- UMLS CUI-4
- C0547047
Description
Date of challenge
Data type
date
Alias
- UMLS CUI [1,1]
- C0011008
- UMLS CUI [1,2]
- C1096479
Description
Provocative concentration resulting in a 20% reduction in FEV1.
Data type
float
Measurement units
- mg/mL
Alias
- UMLS CUI [1,1]
- C1446561
- UMLS CUI [1,2]
- C0001465
- UMLS CUI [2,1]
- C0429706
- UMLS CUI [2,2]
- C0547047
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