ID
41752
Description
Study ID: 103096 Clinical Study ID: 103096 Study Title: A randomised, double blind, placebo controlled, incomplete block, five-way cross-over study to investigate the effect of one week repeat dosing of GW685698X and FP on twenty-four hour serum cortisol in healthy subjects. Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Sponsor: GlaxoSmithKline Phase: Phase 1 Study Recruitment Status: Completed Generic Name: Fluticasone Furoate;Fluticasone Propionate Trade Name: Fluticasone Furoate;Fluticasone Propionate Study Indication: Asthma
Mots-clés
Versions (1)
- 12/01/2021 12/01/2021 -
Détendeur de droits
GlaxoSmithKline
Téléchargé le
12 janvier 2021
DOI
Pour une demande vous connecter.
Licence
Creative Commons BY 4.0
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Effect of one week repeat dosing of GW685698X and FP on serum cortisol (103096)
Screening - Serious Adverse Event; Local Laboratory; Urinalysis; Serology - Screen for HIV Antibody and Hepatitis B & C
Description
Serious Adverse Event
Alias
- UMLS CUI-1
- C1519255
Description
Local Laboratory - Clinical Chemistry
Alias
- UMLS CUI-1
- C0022885
- UMLS CUI-2
- C0008000
Description
Local Laboratory - Clinical Chemistry
Alias
- UMLS CUI-1
- C0022885
- UMLS CUI-2
- C0008000
Description
Clinical Chemistry Test
Type de données
integer
Alias
- UMLS CUI [1]
- C0525044
Description
If the laboratory results meet the protocol definition of an adverse event, record the details on the Non-Seriopus Adverse Events page or Serious Adverse Event page.
Type de données
text
Alias
- UMLS CUI [1,1]
- C0008000
- UMLS CUI [1,2]
- C0587081
Description
Local Laboratory - Haematology
Alias
- UMLS CUI-1
- C0022885
- UMLS CUI-2
- C0018941
Description
Local Laboratory - Haematology
Alias
- UMLS CUI-1
- C0022885
- UMLS CUI-2
- C0474523
Description
Haematology Test
Type de données
integer
Alias
- UMLS CUI [1]
- C0018941
Description
If the laboratory results meet the protocol definition of an adverse event, record the details in the Non-Serious Adverse Events or Serious Adverse Event section(s).
Type de données
text
Alias
- UMLS CUI [1,1]
- C0018941
- UMLS CUI [1,2]
- C1274040
Description
Urinalysis - Local
Alias
- UMLS CUI-1
- C0042014
Description
Date and time sample taken (Urinalysis)
Type de données
datetime
Alias
- UMLS CUI [1,1]
- C0042014
- UMLS CUI [1,2]
- C0200345
- UMLS CUI [1,3]
- C1264639
Description
Result of dipstick
Type de données
text
Alias
- UMLS CUI [1,1]
- C0430370
- UMLS CUI [1,2]
- C0456984
Description
Urinalysis - Local
Alias
- UMLS CUI-1
- C0042014
Description
Urinalysis Test
Type de données
integer
Alias
- UMLS CUI [1]
- C0042014
Description
Urinalysis Test Result
Type de données
text
Alias
- UMLS CUI [1,1]
- C0042014
- UMLS CUI [1,2]
- C1274040
Description
Urinalysis - Microscopy
Alias
- UMLS CUI-1
- C0430397
Description
Urinalysis - Microscopy
Alias
- UMLS CUI-1
- C0430397
Description
Urinalysis Microscopy Test
Type de données
integer
Alias
- UMLS CUI [1]
- C0430397
Description
Complete the Non-Serious Adverse Events (AE) or Serious Adverse Event (SAE) section(s) if clinically significant abnormalities meet the protocol definition for an AE or SAE.
Type de données
text
Alias
- UMLS CUI [1,1]
- C0430397
- UMLS CUI [1,2]
- C0587081
Description
Local Laboratory - Unscheduled Clinical Chemistry
Alias
- UMLS CUI-1
- C0022885
- UMLS CUI-2
- C0008000
- UMLS CUI-3
- C3854240
Description
Local Laboratory - Unscheduled Clinical Chemistry
Alias
- UMLS CUI-1
- C0022885
- UMLS CUI-2
- C0008000
- UMLS CUI-3
- C3854240
Description
Clinical Chemistry Test
Type de données
integer
Alias
- UMLS CUI [1]
- C0525044
Description
If the laboratory results meet the protocol definition of an adverse event, record the details on the Non-Serious Adverse Events page or Serious Adverse Event page.
Type de données
text
Alias
- UMLS CUI [1,1]
- C0008000
- UMLS CUI [1,2]
- C0587081
Description
Local Laboratory - Unscheduled Haematology
Alias
- UMLS CUI-1
- C0022885
- UMLS CUI-2
- C0018941
- UMLS CUI-3
- C3854240
Description
Local Laboratory - Unscheduled Haematology
Alias
- UMLS CUI-1
- C0022885
- UMLS CUI-2
- C0018941
- UMLS CUI-3
- C3854240
Description
Haematology Test
Type de données
integer
Alias
- UMLS CUI [1]
- C0018941
Description
If the laboratory results meet the protocol definition of an adverse event, record the details in the Non-Serious Adverse Events or Serious Adverse Event section(s).
Type de données
text
Alias
- UMLS CUI [1,1]
- C0018941
- UMLS CUI [1,2]
- C1274040
Description
Unscheduled Urinalysis - Local
Alias
- UMLS CUI-1
- C0042014
- UMLS CUI-2
- C3854240
Description
Date and time sample taken (Unscheduled Urinalysis)
Type de données
datetime
Alias
- UMLS CUI [1,1]
- C0042014
- UMLS CUI [1,2]
- C3854240
- UMLS CUI [2,1]
- C0200345
- UMLS CUI [2,2]
- C1264639
Description
Result of dipstick
Type de données
text
Alias
- UMLS CUI [1,1]
- C0430370
- UMLS CUI [1,2]
- C0456984
Description
Unscheduled Urinalysis - Local
Alias
- UMLS CUI-1
- C0042014
- UMLS CUI-2
- C3854240
Description
Urinalysis Test
Type de données
integer
Alias
- UMLS CUI [1]
- C0042014
Description
Urinalysis Test Result
Type de données
text
Alias
- UMLS CUI [1,1]
- C0042014
- UMLS CUI [1,2]
- C1274040
Description
Urinalysis - Microscopy (Unscheduled)
Alias
- UMLS CUI-1
- C0430397
- UMLS CUI-2
- C3854240
Description
Urinalysis - Microscopy (Unscheduled)
Alias
- UMLS CUI-1
- C0430397
- UMLS CUI-2
- C3854240
Description
Urinalysis Microscopy Test
Type de données
integer
Alias
- UMLS CUI [1]
- C0430397
Description
Complete the Non-Serious Adverse Events (AE) or Serious Adverse Event (SAE) section(s) if clinically significant abnormalities meet the protocol definition for an AE or SAE.
Type de données
text
Alias
- UMLS CUI [1,1]
- C0430397
- UMLS CUI [1,2]
- C0587081
Description
Serology - Screen for HIV Antibody and Hepatitis B&C
Alias
- UMLS CUI-1
- C0036743
- UMLS CUI-2
- C0019682
- UMLS CUI-3
- C0019163
- UMLS CUI-4
- C0019196
Description
Date sample taken (Serology)
Type de données
date
Alias
- UMLS CUI [1,1]
- C0036743
- UMLS CUI [1,2]
- C1302413
Description
HIV 1&2 antibodies
Type de données
integer
Alias
- UMLS CUI [1]
- C0019683
Description
Hepatitis B surface antigen
Type de données
integer
Alias
- UMLS CUI [1]
- C0019168
Description
Hepatitis C antibody
Type de données
integer
Alias
- UMLS CUI [1]
- C0201487
Similar models
Screening - Serious Adverse Event; Local Laboratory; Urinalysis; Serology - Screen for HIV Antibody and Hepatitis B & C
C0008000 (UMLS CUI-2)
C0200345 (UMLS CUI [1,2])
C1264639 (UMLS CUI [1,3])
C0008000 (UMLS CUI-2)
C0587081 (UMLS CUI [1,2])
C0018941 (UMLS CUI-2)
C0870078 (UMLS CUI [1,2])
C1264639 (UMLS CUI [1,3])
C0474523 (UMLS CUI-2)
C1274040 (UMLS CUI [1,2])
C0200345 (UMLS CUI [1,2])
C1264639 (UMLS CUI [1,3])
C1274040 (UMLS CUI [1,2])
C2700128 (UMLS CUI [1,2])
C0587081 (UMLS CUI [1,2])
C0008000 (UMLS CUI-2)
C3854240 (UMLS CUI-3)
C3854240 (UMLS CUI [1,2])
C0200345 (UMLS CUI [2,1])
C1264639 (UMLS CUI [2,2])
C0008000 (UMLS CUI-2)
C3854240 (UMLS CUI-3)
C0587081 (UMLS CUI [1,2])
C0018941 (UMLS CUI-2)
C3854240 (UMLS CUI-3)
C3854240 (UMLS CUI [1,2])
C0870078 (UMLS CUI [2,1])
C1264639 (UMLS CUI [2,2])
C0018941 (UMLS CUI-2)
C3854240 (UMLS CUI-3)
C1274040 (UMLS CUI [1,2])
C3854240 (UMLS CUI-2)
C3854240 (UMLS CUI [1,2])
C0200345 (UMLS CUI [2,1])
C1264639 (UMLS CUI [2,2])
C3854240 (UMLS CUI-2)
C1274040 (UMLS CUI [1,2])
C3854240 (UMLS CUI-2)
C2700128 (UMLS CUI [1,2])
C3854240 (UMLS CUI-2)
C0587081 (UMLS CUI [1,2])
C0019682 (UMLS CUI-2)
C0019163 (UMLS CUI-3)
C0019196 (UMLS CUI-4)
C1302413 (UMLS CUI [1,2])