ID
16052
Description
Documentation part: Clinical evaluation & outcome evaluation A Randomised, Observer-blind, Multicentre, Non-inferiority, Comparative, Phase III Study of the Safety and Efficacy of Topical 1% SB-275833 Ointment, Applied Twice Daily for 5 Days, versus Topical 2% Sodium Fusidate Ointment Applied Three Times Daily for 7 Days in the Treatment of Adult and Paediatric Subjects with Impetigo. ClinicalTrials.gov Identifier: NCT00133874 Other Study ID Numbers: TOC100224 Responsible Party: GlaxoSmithKline
Keywords
Versions (3)
- 6/27/16 6/27/16 -
- 4/13/21 4/13/21 - Dr. rer. medic Philipp Neuhaus
- 11/17/21 11/17/21 -
Uploaded on
June 27, 2016
DOI
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License
Creative Commons BY-NC 3.0
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Clinical evaluation & outcome evaluation Topical SB-275833 Ointment 1% For The Treatment Of Impetigo NCT00133874
Clinical evaluation & outcome evaluation Topical SB-275833 Ointment 1% For The Treatment Of Impetigo NCT00133874
Description
Withdrawal
Description
Clinical outcome determination (OUT)
Description
Clinical success
Data type
text
Alias
- UMLS CUI [1]
- C0085565
Description
Clinical failure
Data type
text
Alias
- UMLS CUI [1]
- C3640841
Description
If "Yes", please specify if this was due to Primary or Secondary lesion:
Data type
text
Alias
- UMLS CUI [1,1]
- C3640841
- UMLS CUI [1,2]
- | C1402294
- UMLS CUI [2]
- C1519215
Description
Date of failure
Data type
date
Measurement units
- DDMONYYYY
Alias
- UMLS CUI [1,1]
- C0011008
- UMLS CUI [1,2]
- C3640841
Description
Unable to determine, please specify:
Data type
text
Alias
- UMLS CUI [1,1]
- C0085565
- UMLS CUI [1,2]
- C3845108
Similar models
Clinical evaluation & outcome evaluation Topical SB-275833 Ointment 1% For The Treatment Of Impetigo NCT00133874
| C1402294 (UMLS CUI [1,2])
C1519215 (UMLS CUI [2])
C3640841 (UMLS CUI [1,2])
C3845108 (UMLS CUI [1,2])