ID
35596
Descripción
Study ID: 110978 Clinical Study ID: 110978 Study Title: A Randomized, Double-Blind, Double Dummy, Comparative, Multicenter Study to Assess the Safety and Efficacy of Topical Retapamulin Ointment, 1%, versus Oral Linezolid in the Treatment of Secondarily-Infected Traumatic Lesions and Impetigo Due to Methicillin-Resistant Staphylococcus aureus Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00852540 https://clinicaltrials.gov/ct2/show/NCT00852540 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 3 Study Recruitment Status: Completed Generic Name: Retapamulin Ointment, Oral Linezolid Trade Name: N/A Study Indication: Skin Infections, Bacterial The study consists of 5 vists. The studys period extends over 19 days: Visit 1 (Day 1): Baseline (for both, topical and oral visit) Visit 2 (Day 3-4): On-Therapy (for both, topical and oral visit) Visit 3 (Day 7-9): End of Therapy for topical visit, On-Therapy for oral visit. Visit 4 (Day 12-14): Follow-up for topical visit, End of Therapy for oral visit. Visit 5 (Day 17-19): Final Follow-up for topical visit, Follow-up for oral visit. This document contains the subject diary (For subjects 5-11 years of age; <5 years of age; >=12 years of age) form. It has to be filled in for the end of study. In this Subject Diary, please record the following each day: • the date. • the time that topical medication was applied in the morning. • the time oral suspension medication was taken in the morning. • the time the topical medication was applied in the evening. • the time oral suspension medication was taken in the evening. Please use an ink pen and not a pencil. This medical research study depends on you filling in this diary EVERY DAY. Thank you for your/your child’s participation in this clinical research study. As part of this study, we are asking that, each day, you record in this "Subject Diary" information about how you/your child took the study medication. It is very important that you report in this diary the dosing information for each day that you/your child took study medication. Please bring this diary with you to each of your appointments, until the diary is collected by the study site staff. Following your/your child’s treatment, please return ALL medication tubes and bottles to the study coordinator who gave you the study medication. Thank you very much for your help.
Link
https://clinicaltrials.gov/ct2/show/NCT00852540
Palabras clave
Versiones (2)
- 4/3/19 4/3/19 -
- 11/3/19 11/3/19 -
Titular de derechos de autor
GlaxoSmithKline
Subido en
11 de marzo de 2019
DOI
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Licencia
Creative Commons BY-NC 3.0
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Safety and efficacy of topical Retapamulin Ointment vs. oral Linezolid in Secondarily-Infected Traumatic Lesions and Impetigo due to MRSA, NCT00852540
Subject Diary
- StudyEvent: ODM
Descripción
Subject diary instruction
Alias
- UMLS CUI-1
- C3890583
- UMLS CUI-2
- C1442085
Descripción
Should you have any questions about the study medication prior to your next appointment, please contact your study coordinator (see below).
Tipo de datos
text
Alias
- UMLS CUI [1]
- C0337611
Descripción
Contact details
Tipo de datos
text
Alias
- UMLS CUI [1]
- C1522508
Descripción
Medication
Alias
- UMLS CUI-1
- C0013227
Descripción
Study medication
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0013227
Descripción
For oral medication please fill in on all days. For topical medication fill in only on day 1 - day 6.
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C0013227
- UMLS CUI [1,2]
- C0439228
Descripción
day month year
Tipo de datos
date
Alias
- UMLS CUI [1,1]
- C0013227
- UMLS CUI [1,2]
- C0011008
Descripción
24-hr clock
Tipo de datos
time
Alias
- UMLS CUI [1,1]
- C0013227
- UMLS CUI [1,2]
- C0040223
- UMLS CUI [1,3]
- C0332170
Descripción
24-hr clock
Tipo de datos
time
Alias
- UMLS CUI [1,1]
- C0013227
- UMLS CUI [1,2]
- C0040223
- UMLS CUI [1,3]
- C0587117
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Subject Diary
- StudyEvent: ODM
C0600091 (UMLS CUI [1,2])
C1442085 (UMLS CUI-2)
C0439228 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
C0040223 (UMLS CUI [1,2])
C0332170 (UMLS CUI [1,3])
C0040223 (UMLS CUI [1,2])
C0587117 (UMLS CUI [1,3])