ID
44766
Beskrivning
Documentation part: Adverse Events & Clinical 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
Nyckelord
Versioner (4)
- 2016-06-27 2016-06-27 -
- 2016-06-27 2016-06-27 -
- 2021-04-13 2021-04-13 - Dr. rer. medic Philipp Neuhaus
- 2021-11-17 2021-11-17 -
Rättsinnehavare
GlaxoSmithKline
Uppladdad den
17 november 2021
DOI
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Licens
Creative Commons BY-NC 4.0
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Adverse Events & Clinical Outcome Evaluation Topical SB-275833 Ointment 1% For The Treatment Of Impetigo NCT00133874
Adverse Events & Clinical Outcome Evaluation Topical SB-275833 Ointment 1% For The Treatment Of Impetigo NCT00133874
Beskrivning
Clinical Outcome Determination (OUT)
Beskrivning
Clinical success
Datatyp
text
Alias
- UMLS CUI [1]
- C0085565
Beskrivning
Clinical recurrence
Datatyp
text
Alias
- UMLS CUI [1]
- C0679254
Beskrivning
If
Datatyp
text
Alias
- UMLS CUI [1,1]
- C3640841
- UMLS CUI [1,2]
- C1402294
- UMLS CUI [2,1]
- C3640841
- UMLS CUI [2,2]
- C1519215
Beskrivning
Date of recurrence
Datatyp
date
Måttenheter
- DDMONYYYY
Alias
- UMLS CUI [1]
- C0807712
Beskrivning
Unable to determine clinical outcome, please specify:
Datatyp
text
Alias
- UMLS CUI [1,1]
- C0085565
- UMLS CUI [1,2]
- C3845108
Similar models
Adverse Events & Clinical Outcome Evaluation Topical SB-275833 Ointment 1% For The Treatment Of Impetigo NCT00133874
C1522314 (UMLS CUI [2])
C1301931 (UMLS CUI [2])
C0877248 (UMLS CUI [1,2])
C0877248 (UMLS CUI [1,2])
C1710056 (UMLS CUI [1,2])
C3641099 (UMLS CUI [1,2])
C1402294 (UMLS CUI [1,2])
C3640841 (UMLS CUI [2,1])
C1519215 (UMLS CUI [2,2])
C3845108 (UMLS CUI [1,2])
Inga kommentarer