ID

44767

Beschrijving

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

Trefwoorden

  1. 27-06-16 27-06-16 -
  2. 13-04-21 13-04-21 - Dr. rer. medic Philipp Neuhaus
  3. 17-11-21 17-11-21 -
Houder van rechten

GlaxoSmithKline

Geüploaded op

17 november 2021

DOI

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Licentie

Creative Commons BY-NC 4.0

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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

Clinical Evaluation
Beschrijving

Clinical Evaluation

Clinical Evaluation
Beschrijving

Clinical Evaluation

Datatype

text

Alias
UMLS CUI [1]
C1261322
Withdrawal
Beschrijving

Withdrawal

Is the subject withdrawing from treatment at this visit?
Beschrijving

Is the subject withdrawing from treatment at this visit?

Datatype

text

Alias
UMLS CUI [1]
C0422727
Clinical outcome determination (OUT)
Beschrijving

Clinical outcome determination (OUT)

Clinical success
Beschrijving

Clinical success

Datatype

text

Alias
UMLS CUI [1]
C0085565
Clinical failure
Beschrijving

Clinical failure

Datatype

text

Alias
UMLS CUI [1]
C3640841
If "Yes", please specify if this was due to Primary or Secondary lesion:
Beschrijving

If

Datatype

text

Alias
UMLS CUI [1,1]
C3640841
UMLS CUI [1,2]
C1402294
UMLS CUI [2,1]
C3640841
UMLS CUI [2,2]
C1519215
Date of failure
Beschrijving

Date of failure

Datatype

date

Maateenheden
  • DDMONYYYY
Alias
UMLS CUI [1,1]
C0011008
UMLS CUI [1,2]
C3640841
DDMONYYYY
Unable to determine, please specify:
Beschrijving

Unable to determine, please specify:

Datatype

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

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
Clinical Evaluation
Item
Clinical Evaluation
text
C1261322 (UMLS CUI [1])
Code List
Clinical Evaluation
CL Item
Improvement (1)
CL Item
Worsening (2)
CL Item
No change (3)
Item Group
Withdrawal
Item
Is the subject withdrawing from treatment at this visit?
text
C0422727 (UMLS CUI [1])
Code List
Is the subject withdrawing from treatment at this visit?
CL Item
Yes (Y)
CL Item
No (N)
Item Group
Clinical outcome determination (OUT)
Item
Clinical success
text
C0085565 (UMLS CUI [1])
Code List
Clinical success
CL Item
Yes (Y)
CL Item
No (N)
Item
Clinical failure
text
C3640841 (UMLS CUI [1])
Code List
Clinical failure
CL Item
Yes (Y)
CL Item
No (N)
Item
If "Yes", please specify if this was due to Primary or Secondary lesion:
text
C3640841 (UMLS CUI [1,1])
C1402294 (UMLS CUI [1,2])
C3640841 (UMLS CUI [2,1])
C1519215 (UMLS CUI [2,2])
Code List
If "Yes", please specify if this was due to Primary or Secondary lesion:
CL Item
Primary lesion (P)
CL Item
Secondary lesion (S)
Date of failure
Item
Date of failure
date
C0011008 (UMLS CUI [1,1])
C3640841 (UMLS CUI [1,2])
Unable to determine, please specify:
Item
Unable to determine, please specify:
text
C0085565 (UMLS CUI [1,1])
C3845108 (UMLS CUI [1,2])

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