ID

41961

Beschrijving

Study ID: 110159 Clinical Study ID: 110159 Study Title: A Randomised, Double-Blind, Placebo-Controlled, 3-Period Crossover Study to Assess the Efficacy and Safety of Single Dose Intranasal GSK1004723 Compared With Placebo in an Allergen Challenge Chamber in Male Subjects With Seasonal Allergic Rhinitis Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00824356 Sponsor: GlaxoSmithKline Phase: Phase 2 Study Recruitment Status: Completed Generic Name: Placebo, GSK1004723 (200mg), GSK1004723 (1000mg) Study Indication: Allergic Rhinitis

Trefwoorden

Versies (3)
  1. 22-02-21 22-02-21 -
  2. 22-02-21 22-02-21 -
  3. 25-02-21 25-02-21 -
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GlaxoSmithKline

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22 februari 2021

DOI

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Creative Commons BY 4.0
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Efficacy and Safety of Single Dose Intranasal GSK1004723 in an Allergen Challenge Chamber NCT00824356

Engels

Visit 1 - Randomisation Number; Vital Signs; Nasal Inspection; Challenge Date and Time; Investigational Product

1 Formulieren  
Date of Visit
Beschrijving

Date of Visit

Alias
UMLS CUI-1
C1320303
Date of visit/assessment
Beschrijving

Date of visit/assessment

Datatype

date

Alias
UMLS CUI [1]
C1320303
UMLS CUI [2]
C2985720
Randomisation Number
Beschrijving

Randomisation Number

Alias
UMLS CUI-1
C0034656
UMLS CUI-2
C0237753
Was the subject able to be randomised?
Beschrijving

Was the subject able to be randomised?

Datatype

boolean

Alias
UMLS CUI [1]
C0034656
Provide Randomisation number
Beschrijving

Provide Randomisation number

Datatype

text

Alias
UMLS CUI [1,1]
C0034656
UMLS CUI [1,2]
C0237753
Vital Signs - Challenge Date and Time
Beschrijving

Vital Signs - Challenge Date and Time

Alias
UMLS CUI-1
C0518766
UMLS CUI-2
C0805586
UMLS CUI-3
C1264639
Vital Signs - Challenge date/time
Beschrijving

Vital Signs - Challenge date/time

Datatype

datetime

Alias
UMLS CUI [1]
C0518766
UMLS CUI [2,1]
C0805586
UMLS CUI [2,2]
C1264639
Vital Signs - Start of Challenge
Beschrijving

Vital Signs - Start of Challenge

Alias
UMLS CUI-1
C0518766
UMLS CUI-2
C0805586
UMLS CUI-3
C0808070
Start of Challenge - Actual date/time
Beschrijving

Start of Challenge - Actual date/time

Datatype

datetime

Alias
UMLS CUI [1,1]
C0805586
UMLS CUI [1,2]
C0808070
UMLS CUI [2]
C1264639
Start of Challenge - Systolic Blood Pressure
Beschrijving

Start of Challenge - Systolic Blood Pressure

Datatype

integer

Maateenheden
  • mm[Hg]
Alias
UMLS CUI [1,1]
C0805586
UMLS CUI [1,2]
C0808070
UMLS CUI [1,3]
C0871470
mm[Hg]
Start of Challenge - Diastolic Blood Pressure
Beschrijving

Start of Challenge - Diastolic Blood Pressure

Datatype

integer

Maateenheden
  • mm[Hg]
Alias
UMLS CUI [1,1]
C0805586
UMLS CUI [1,2]
C0808070
UMLS CUI [1,3]
C0428883
mm[Hg]
Start of Challenge - Heart rate
Beschrijving

Start of Challenge - Heart rate

Datatype

integer

Maateenheden
  • beats/min
Alias
UMLS CUI [1,1]
C0805586
UMLS CUI [1,2]
C0808070
UMLS CUI [1,3]
C0018810
beats/min
Challenge Date and Time - Challenge (0 - 6 Hr)
Beschrijving

Challenge Date and Time - Challenge (0 - 6 Hr)

Alias
UMLS CUI-1
C0805586
UMLS CUI-2
C1264639
Challenge (0 - 6 Hr) - Start date/time of challenge
Beschrijving

Challenge (0 - 6 Hr) - Start date/time of challenge

Datatype

datetime

Alias
UMLS CUI [1,1]
C0805586
UMLS CUI [1,2]
C0808070
UMLS CUI [2,1]
C0805586
UMLS CUI [2,2]
C1301880
Challenge (0 - 6 Hr) - End time of challenge
Beschrijving

Challenge (0 - 6 Hr) - End time of challenge

Datatype

time

Alias
UMLS CUI [1,1]
C0805586
UMLS CUI [1,2]
C1522314
Investigational Product (Dose) - Challenge Date and Time
Beschrijving

Investigational Product (Dose) - Challenge Date and Time

Alias
UMLS CUI-1
C0304229
UMLS CUI-2
C0678766
UMLS CUI-3
C0805586
UMLS CUI-4
C1264639
Investigational Product (Dose) - Challenge Date/Time
Beschrijving

Investigational Product (Dose) - Challenge Date/Time

Datatype

datetime

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0678766
UMLS CUI [2,1]
C0805586
UMLS CUI [2,2]
C1264639
Investigational Product - Date/time of dose
Beschrijving

Investigational Product - Date/time of dose

Alias
UMLS CUI-1
C0304229
UMLS CUI-2
C0178602
UMLS CUI-3
C1264639
Investigational Product - Date/time of dose
Beschrijving

Investigational Product - Date/time of dose

Datatype

datetime

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1264639
Investigational Product - Treatment Confirmation
Beschrijving

Investigational Product - Treatment Confirmation

Alias
UMLS CUI-1
C0304229
UMLS CUI-2
C0087111
UMLS CUI-3
C0750484
Did the subject receive the correct treatment (e.g., treatment which the subject was assigned to) during this dosing interval?
Beschrijving

Did the subject receive the correct treatment (e.g., treatment which the subject was assigned to) during this dosing interval?

Datatype

boolean

Alias
UMLS CUI [1,1]
C0750484
UMLS CUI [1,2]
C0087111
If subject did not receive the correct treatment, record reason
Beschrijving

If subject did not receive the correct treatment, record reason

Datatype

text

Alias
UMLS CUI [1,1]
C0087111
UMLS CUI [1,2]
C2349182
UMLS CUI [1,3]
C0392360
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Similar models

Visit 1 - Randomisation Number; Vital Signs; Nasal Inspection; Challenge Date and Time; Investigational Product

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
Date of Visit
C1320303 (UMLS CUI-1)
Date of visit/assessment
Item
Date of visit/assessment
date
C1320303 (UMLS CUI [1])
C2985720 (UMLS CUI [2])
Item Group
Randomisation Number
C0034656 (UMLS CUI-1)
C0237753 (UMLS CUI-2)
Was the subject able to be randomised?
Item
Was the subject able to be randomised?
boolean
C0034656 (UMLS CUI [1])
Provide Randomisation number
Item
Provide Randomisation number
text
C0034656 (UMLS CUI [1,1])
C0237753 (UMLS CUI [1,2])
Item Group
Vital Signs - Challenge Date and Time
C0518766 (UMLS CUI-1)
C0805586 (UMLS CUI-2)
C1264639 (UMLS CUI-3)
Vital Signs - Challenge date/time
Item
Vital Signs - Challenge date/time
datetime
C0518766 (UMLS CUI [1])
C0805586 (UMLS CUI [2,1])
C1264639 (UMLS CUI [2,2])
Item Group
Vital Signs - Start of Challenge
C0518766 (UMLS CUI-1)
C0805586 (UMLS CUI-2)
C0808070 (UMLS CUI-3)
Start of Challenge - Actual date/time
Item
Start of Challenge - Actual date/time
datetime
C0805586 (UMLS CUI [1,1])
C0808070 (UMLS CUI [1,2])
C1264639 (UMLS CUI [2])
Start of Challenge - Systolic Blood Pressure
Item
Start of Challenge - Systolic Blood Pressure
integer
C0805586 (UMLS CUI [1,1])
C0808070 (UMLS CUI [1,2])
C0871470 (UMLS CUI [1,3])
Start of Challenge - Diastolic Blood Pressure
Item
Start of Challenge - Diastolic Blood Pressure
integer
C0805586 (UMLS CUI [1,1])
C0808070 (UMLS CUI [1,2])
C0428883 (UMLS CUI [1,3])
Start of Challenge - Heart rate
Item
Start of Challenge - Heart rate
integer
C0805586 (UMLS CUI [1,1])
C0808070 (UMLS CUI [1,2])
C0018810 (UMLS CUI [1,3])
Item Group
Challenge Date and Time - Challenge (0 - 6 Hr)
C0805586 (UMLS CUI-1)
C1264639 (UMLS CUI-2)
Challenge (0 - 6 Hr) - Start date/time of challenge
Item
Challenge (0 - 6 Hr) - Start date/time of challenge
datetime
C0805586 (UMLS CUI [1,1])
C0808070 (UMLS CUI [1,2])
C0805586 (UMLS CUI [2,1])
C1301880 (UMLS CUI [2,2])
Challenge (0 - 6 Hr) - End time of challenge
Item
Challenge (0 - 6 Hr) - End time of challenge
time
C0805586 (UMLS CUI [1,1])
C1522314 (UMLS CUI [1,2])
Item Group
Investigational Product (Dose) - Challenge Date and Time
C0304229 (UMLS CUI-1)
C0678766 (UMLS CUI-2)
C0805586 (UMLS CUI-3)
C1264639 (UMLS CUI-4)
Investigational Product (Dose) - Challenge Date/Time
Item
Investigational Product (Dose) - Challenge Date/Time
datetime
C0304229 (UMLS CUI [1,1])
C0678766 (UMLS CUI [1,2])
C0805586 (UMLS CUI [2,1])
C1264639 (UMLS CUI [2,2])
Item Group
Investigational Product - Date/time of dose
C0304229 (UMLS CUI-1)
C0178602 (UMLS CUI-2)
C1264639 (UMLS CUI-3)
Investigational Product - Date/time of dose
Item
Investigational Product - Date/time of dose
datetime
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1264639 (UMLS CUI [1,3])
Item Group
Investigational Product - Treatment Confirmation
C0304229 (UMLS CUI-1)
C0087111 (UMLS CUI-2)
C0750484 (UMLS CUI-3)
Did the subject receive the correct treatment (e.g., treatment which the subject was assigned to) during this dosing interval?
Item
Did the subject receive the correct treatment (e.g., treatment which the subject was assigned to) during this dosing interval?
boolean
C0750484 (UMLS CUI [1,1])
C0087111 (UMLS CUI [1,2])
If subject did not receive the correct treatment, record reason
Item
If subject did not receive the correct treatment, record reason
text
C0087111 (UMLS CUI [1,1])
C2349182 (UMLS CUI [1,2])
C0392360 (UMLS CUI [1,3])
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