ID

29673

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, Methacholine Challenge. Time: Treatment Period 1, Day 29.

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 1, Day 29

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
Pulmonary function tests: Pre-Methacholine Challenge
Description

Pulmonary function tests: Pre-Methacholine Challenge

Alias
UMLS CUI-1
C0024119
UMLS CUI-2
C0430567
UMLS CUI-3
C3812758
pre-Methacholine pulmonary function test date
Description

pre-Methacholine pulmonary function test date

Data type

date

Alias
UMLS CUI [1,1]
C0011008
UMLS CUI [1,2]
C0024119
UMLS CUI [1,3]
C0430567
UMLS CUI [1,4]
C3812758
Planned relative Time
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
Time of FEV1
Description

Time of FEV1

Data type

time

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

FEV1 Reading

Data type

float

Measurement units
  • L
Alias
UMLS CUI [1,1]
C0456984
UMLS CUI [1,2]
C0429706
L
Pulmonary function tests: Methacholine Challenge
Description

Pulmonary function tests: Methacholine Challenge

Alias
UMLS CUI-1
C0748133
UMLS CUI-2
C0430567
Methacholine Challenge Date
Description

Methacholine Challenge Date

Data type

date

Alias
UMLS CUI [1,1]
C0011008
UMLS CUI [1,2]
C0748133
UMLS CUI [1,3]
C0430567
Inhaled Substance
Description

Inhaled Substance

Data type

text

Alias
UMLS CUI [1,1]
C0205535
UMLS CUI [1,2]
C0600370
UMLS CUI [2,1]
C0205535
UMLS CUI [2,2]
C0036082
Challenge Concentration (New Subjects)
Description

Following the baseline assessment in which FEV1 is measured after inhalation of saline, subjects are to inhale doubling increments of Methacoline (provocholine) until a ≥20 percent 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]
C0600370
Challenge Concentration (Historical concentration)
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 Methacholine (provocholine) 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]
C0600370
mg/mL
Start Time of Inhalation
Description

Fill in only for saline inhalation and new subjects.

Data type

time

Alias
UMLS CUI [1,1]
C1301880
UMLS CUI [1,2]
C0001559
Stop Time of Inhalation
Description

Stop Time of Inhalation

Data type

time

Alias
UMLS CUI [1,1]
C1522314
UMLS CUI [1,2]
C0001559
Planned relative Time of FEV1
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
Pulmonary function time
Description

Pulmonary function time

Data type

time

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

FEV1 Result

Data type

float

Measurement units
  • L
Alias
UMLS CUI [1,1]
C0429706
UMLS CUI [1,2]
C0430567
L
Pulmonary function tests: Post-Methacholine Challenge
Description

Pulmonary function tests: Post-Methacholine Challenge

Alias
UMLS CUI-1
C0231921
UMLS CUI-2
C0430567
UMLS CUI-3
C0439568
Date of post-challenge FEV1
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
Time of post-challenge FEV1
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
Result of post-challenge FEV1
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
L
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Similar models

Lung function testing - Treatment Period 1, Day 29

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
unscheduled (unscheduled)
(Comment:en)
CL Item
within 1 hr post-challenge (within 1 hr post-challenge)
(Comment:en)
CL Item
pre-challenge (pre-challenge)
(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
unscheduled (unscheduled)
(Comment:en)
CL Item
pre-challenge (pre-challenge)
(Comment:en)
CL Item
post-challenge (discharge) (post-challenge (discharge))
(Comment:en)
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])
Item Group
Pulmonary function tests: Pre-Methacholine Challenge
C0024119 (UMLS CUI-1)
C0430567 (UMLS CUI-2)
C3812758 (UMLS CUI-3)
pre-Methacholine pulmonary function test date
Item
pre-Methacholine pulmonary function test date
date
C0011008 (UMLS CUI [1,1])
C0024119 (UMLS CUI [1,2])
C0430567 (UMLS CUI [1,3])
C3812758 (UMLS CUI [1,4])
Item
Planned relative Time
text
C0439564 (UMLS CUI [1,1])
C0748133 (UMLS CUI [1,2])
Planned relative Time
Code List
Planned relative Time
CL Item
pre-saline (pre-saline)
CL Item
unscheduled (unscheduled)
Time of FEV1
Item
Time of FEV1
time
C0040223 (UMLS CUI [1,1])
C0429706 (UMLS CUI [1,2])
FEV1 Reading
Item
FEV1 Reading
float
C0456984 (UMLS CUI [1,1])
C0429706 (UMLS CUI [1,2])
Item Group
Pulmonary function tests: Methacholine Challenge
C0748133 (UMLS CUI-1)
C0430567 (UMLS CUI-2)
Methacholine Challenge Date
Item
Methacholine Challenge Date
date
C0011008 (UMLS CUI [1,1])
C0748133 (UMLS CUI [1,2])
C0430567 (UMLS CUI [1,3])
Item
Inhaled Substance
text
C0205535 (UMLS CUI [1,1])
C0600370 (UMLS CUI [1,2])
C0205535 (UMLS CUI [2,1])
C0036082 (UMLS CUI [2,2])
Inhaled Substance
Code List
Inhaled Substance
CL Item
Saline (Saline)
CL Item
Saline, unscheduled (Saline, unscheduled)
CL Item
Metacholine (Metacholine)
Item
Challenge Concentration (New Subjects)
text
C1446561 (UMLS CUI [1,1])
C0600370 (UMLS CUI [1,2])
Challenge Concentration (New Subjects)
Code List
Challenge Concentration (New Subjects)
CL Item
0.000 (0.000)
CL Item
0.03125 (0.03125)
CL Item
0.06250 (0.06250)
CL Item
0.125 (0.125)
CL Item
0.25 (0.25)
CL Item
0.5 (0.5)
CL Item
1 (1)
CL Item
2 (2)
CL Item
4 (4)
CL Item
8 (8)
CL Item
16 (16)
CL Item
32 (32)
Challenge Concentration (Historical concentration)
Item
Challenge Concentration (Historical concentration)
float
C1446561 (UMLS CUI [1,1])
C0600370 (UMLS CUI [1,2])
Start Time of Inhalation
Item
Start Time of Inhalation
time
C1301880 (UMLS CUI [1,1])
C0001559 (UMLS CUI [1,2])
Stop Time of Inhalation
Item
Stop Time of Inhalation
time
C1522314 (UMLS CUI [1,1])
C0001559 (UMLS CUI [1,2])
Item
Planned relative Time of FEV1
text
C0439564 (UMLS CUI [1,1])
C0205535 (UMLS CUI [1,2])
C0748133 (UMLS CUI [1,3])
Planned relative Time of FEV1
Code List
Planned relative Time of FEV1
CL Item
60 secs post-inhalation (60 secs post-inhalation)
CL Item
180 secs post-inhalation (180 secs post-inhalation)
Pulmonary function time
Item
Pulmonary function time
time
C0040223 (UMLS CUI [1,1])
C0429706 (UMLS CUI [1,2])
FEV1 Result
Item
FEV1 Result
float
C0429706 (UMLS CUI [1,1])
C0430567 (UMLS CUI [1,2])
Item Group
Pulmonary function tests: Post-Methacholine Challenge
C0231921 (UMLS CUI-1)
C0430567 (UMLS CUI-2)
C0439568 (UMLS CUI-3)
Date of post-challenge FEV1
Item
Date of post-challenge FEV1
date
C0011008 (UMLS CUI [1,1])
C0429706 (UMLS CUI [1,2])
C0439568 (UMLS CUI [1,3])
Time of post-challenge FEV1
Item
Time of post-challenge FEV1
time
C0040223 (UMLS CUI [1,1])
C0429706 (UMLS CUI [1,2])
C0439568 (UMLS CUI [1,3])
Result of post-challenge FEV1
Item
Result of post-challenge FEV1
float
C0429706 (UMLS CUI [1,1])
C1274040 (UMLS CUI [1,2])
C0439568 (UMLS CUI [1,3])
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