ID
41961
Description
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
Mots-clés
Versions (3)
- 22/02/2021 22/02/2021 -
- 22/02/2021 22/02/2021 -
- 25/02/2021 25/02/2021 -
Détendeur de droits
GlaxoSmithKline
Téléchargé le
22 février 2021
DOI
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Licence
Creative Commons BY 4.0
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Efficacy and Safety of Single Dose Intranasal GSK1004723 in an Allergen Challenge Chamber NCT00824356
Visit 1 - Randomisation Number; Vital Signs; Nasal Inspection; Challenge Date and Time; Investigational Product
Description
Randomisation Number
Alias
- UMLS CUI-1
- C0034656
- UMLS CUI-2
- C0237753
Description
Vital Signs - Challenge Date and Time
Alias
- UMLS CUI-1
- C0518766
- UMLS CUI-2
- C0805586
- UMLS CUI-3
- C1264639
Description
Vital Signs - Start of Challenge
Alias
- UMLS CUI-1
- C0518766
- UMLS CUI-2
- C0805586
- UMLS CUI-3
- C0808070
Description
Start of Challenge - Actual date/time
Type de données
datetime
Alias
- UMLS CUI [1,1]
- C0805586
- UMLS CUI [1,2]
- C0808070
- UMLS CUI [2]
- C1264639
Description
Start of Challenge - Systolic Blood Pressure
Type de données
integer
Unités de mesure
- mm[Hg]
Alias
- UMLS CUI [1,1]
- C0805586
- UMLS CUI [1,2]
- C0808070
- UMLS CUI [1,3]
- C0871470
Description
Start of Challenge - Diastolic Blood Pressure
Type de données
integer
Unités de mesure
- mm[Hg]
Alias
- UMLS CUI [1,1]
- C0805586
- UMLS CUI [1,2]
- C0808070
- UMLS CUI [1,3]
- C0428883
Description
Start of Challenge - Heart rate
Type de données
integer
Unités de mesure
- beats/min
Alias
- UMLS CUI [1,1]
- C0805586
- UMLS CUI [1,2]
- C0808070
- UMLS CUI [1,3]
- C0018810
Description
Challenge Date and Time - Challenge (0 - 6 Hr)
Alias
- UMLS CUI-1
- C0805586
- UMLS CUI-2
- C1264639
Description
Challenge (0 - 6 Hr) - Start date/time of challenge
Type de données
datetime
Alias
- UMLS CUI [1,1]
- C0805586
- UMLS CUI [1,2]
- C0808070
- UMLS CUI [2,1]
- C0805586
- UMLS CUI [2,2]
- C1301880
Description
Challenge (0 - 6 Hr) - End time of challenge
Type de données
time
Alias
- UMLS CUI [1,1]
- C0805586
- UMLS CUI [1,2]
- C1522314
Description
Investigational Product (Dose) - Challenge Date and Time
Alias
- UMLS CUI-1
- C0304229
- UMLS CUI-2
- C0678766
- UMLS CUI-3
- C0805586
- UMLS CUI-4
- C1264639
Description
Investigational Product - Date/time of dose
Alias
- UMLS CUI-1
- C0304229
- UMLS CUI-2
- C0178602
- UMLS CUI-3
- C1264639
Description
Investigational Product - Treatment Confirmation
Alias
- UMLS CUI-1
- C0304229
- UMLS CUI-2
- C0087111
- UMLS CUI-3
- C0750484
Description
Did the subject receive the correct treatment (e.g., treatment which the subject was assigned to) during this dosing interval?
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0750484
- UMLS CUI [1,2]
- C0087111
Description
If subject did not receive the correct treatment, record reason
Type de données
text
Alias
- UMLS CUI [1,1]
- C0087111
- UMLS CUI [1,2]
- C2349182
- UMLS CUI [1,3]
- C0392360
Similar models
Visit 1 - Randomisation Number; Vital Signs; Nasal Inspection; Challenge Date and Time; Investigational Product
C2985720 (UMLS CUI [2])
C0237753 (UMLS CUI [1,2])
C0805586 (UMLS CUI-2)
C1264639 (UMLS CUI-3)
C0805586 (UMLS CUI [2,1])
C1264639 (UMLS CUI [2,2])
C0805586 (UMLS CUI-2)
C0808070 (UMLS CUI-3)
C0808070 (UMLS CUI [1,2])
C1264639 (UMLS CUI [2])
C0808070 (UMLS CUI [1,2])
C0871470 (UMLS CUI [1,3])
C0808070 (UMLS CUI [1,2])
C0428883 (UMLS CUI [1,3])
C0808070 (UMLS CUI [1,2])
C0018810 (UMLS CUI [1,3])
C1264639 (UMLS CUI-2)
C0808070 (UMLS CUI [1,2])
C0805586 (UMLS CUI [2,1])
C1301880 (UMLS CUI [2,2])
C1522314 (UMLS CUI [1,2])
C0678766 (UMLS CUI-2)
C0805586 (UMLS CUI-3)
C1264639 (UMLS CUI-4)
C0678766 (UMLS CUI [1,2])
C0805586 (UMLS CUI [2,1])
C1264639 (UMLS CUI [2,2])
C0178602 (UMLS CUI-2)
C1264639 (UMLS CUI-3)
C0178602 (UMLS CUI [1,2])
C1264639 (UMLS CUI [1,3])
C0087111 (UMLS CUI-2)
C0750484 (UMLS CUI-3)
C0087111 (UMLS CUI [1,2])
C2349182 (UMLS CUI [1,2])
C0392360 (UMLS CUI [1,3])