ID

29668

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 2, Day 28.

Link

https://clinicaltrials.gov/ct2/show/NCT00318630

Keywords

Versions (1)
  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

English

Lung function testing - Treatment Period 2, Day 28

1 forms  
Exhaled nitric oxide
Description

Exhaled nitric oxide

Alias
UMLS CUI-1
C3700245
Date of Exhaled nitric oxide test
Description

e.g., 08 JAN 04

Data type

date

Alias
UMLS CUI [1,1]
C3700245
UMLS CUI [1,2]
C2826247
Planned relative time
Description

Time relative to dosing

Data type

text

Alias
UMLS CUI [1]
C0439564
Actual time of first reading
Description

hr:min 00:00 - 23:59

Data type

time

Alias
UMLS CUI [1,1]
C0040223
UMLS CUI [1,2]
C3700245
Reading 1 of Nictric Oxide
Description

e.g., 50.7

Data type

float

Measurement units
  • ppb
Alias
UMLS CUI [1,1]
C0028128
UMLS CUI [1,2]
C0456984
ppb
Reading 2 of Nictric Oxide
Description

e.g., 51.0

Data type

float

Measurement units
  • ppb
Alias
UMLS CUI [1,1]
C0028128
UMLS CUI [1,2]
C0456984
ppb
Reading 3 of Nictric Oxide
Description

e.g., 51.3

Data type

float

Measurement units
  • ppb
Alias
UMLS CUI [1,1]
C0028128
UMLS CUI [1,2]
C0456984
ppb
Pulmonary function tests / FEV 1
Description

Pulmonary function tests / FEV 1

Alias
UMLS CUI-1
C0024119
UMLS CUI-2
C0429706
Date of FEV1
Description

Date of FEV1

Data type

date

Alias
UMLS CUI [1,1]
C0011008
UMLS CUI [1,2]
C0429706
Planned relative Time of FEV1
Description

Time relative to Dosing.

Data type

text

Alias
UMLS CUI [1,1]
C0439564
UMLS CUI [1,2]
C0429706
Time of FEV1
Description

Hr : Min 00:00-23:59

Data type

time

Alias
UMLS CUI [1,1]
C0040223
UMLS CUI [1,2]
C0429706
Reading 1 of FEV1
Description

Reading 1 of FEV1

Data type

float

Measurement units
  • L
Alias
UMLS CUI [1,1]
C0456984
UMLS CUI [1,2]
C0429706
L
Reading 2 of FEV1
Description

Reading 2 of FEV1

Data type

float

Measurement units
  • L
Alias
UMLS CUI [1,1]
C0456984
UMLS CUI [1,2]
C0429706
L
Reading 3 of FEV1
Description

Reading 3 of FEV1

Data type

float

Measurement units
  • L
Alias
UMLS CUI [1,1]
C0456984
UMLS CUI [1,2]
C0429706
L
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Similar models

Lung function testing - Treatment Period 2, Day 28

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Exhaled nitric oxide
C3700245 (UMLS CUI-1)
Date of Exhaled nitric oxide test
Item
Date of Exhaled nitric oxide test
date
C3700245 (UMLS CUI [1,1])
C2826247 (UMLS CUI [1,2])
Item
Planned relative time
text
C0439564 (UMLS CUI [1])
Planned relative time
Code List
Planned relative time
CL Item
pre-dose (pre-dose)
(Comment:en)
CL Item
unscheduled (unscheduled)
(Comment:en)
Actual time of first reading
Item
Actual time of first reading
time
C0040223 (UMLS CUI [1,1])
C3700245 (UMLS CUI [1,2])
Reading 1 of Nictric Oxide
Item
Reading 1 of Nictric Oxide
float
C0028128 (UMLS CUI [1,1])
C0456984 (UMLS CUI [1,2])
Reading 2 of Nictric Oxide
Item
Reading 2 of Nictric Oxide
float
C0028128 (UMLS CUI [1,1])
C0456984 (UMLS CUI [1,2])
Reading 3 of Nictric Oxide
Item
Reading 3 of Nictric Oxide
float
C0028128 (UMLS CUI [1,1])
C0456984 (UMLS CUI [1,2])
Item Group
Pulmonary function tests / FEV 1
C0024119 (UMLS CUI-1)
C0429706 (UMLS CUI-2)
Date of FEV1
Item
Date of FEV1
date
C0011008 (UMLS CUI [1,1])
C0429706 (UMLS CUI [1,2])
Item
Planned relative Time of FEV1
text
C0439564 (UMLS CUI [1,1])
C0429706 (UMLS CUI [1,2])
Planned relative Time of FEV1
Code List
Planned relative Time of FEV1
CL Item
pre-dose (pre-dose)
CL Item
post-dose (discharge) (post-dose (discharge))
CL Item
unscheduled (unscheduled)
Time of FEV1
Item
Time of FEV1
time
C0040223 (UMLS CUI [1,1])
C0429706 (UMLS CUI [1,2])
Reading 1 of FEV1
Item
Reading 1 of FEV1
float
C0456984 (UMLS CUI [1,1])
C0429706 (UMLS CUI [1,2])
Reading 2 of FEV1
Item
Reading 2 of FEV1
float
C0456984 (UMLS CUI [1,1])
C0429706 (UMLS CUI [1,2])
Reading 3 of FEV1
Item
Reading 3 of FEV1
float
C0456984 (UMLS CUI [1,1])
C0429706 (UMLS CUI [1,2])
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