ID
35421
Beschreibung
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.
Link
https://clinicaltrials.gov/ct2/show/NCT00852540
Stichworte
Versionen (2)
- 04.03.19 04.03.19 -
- 11.03.19 11.03.19 -
Rechteinhaber
GlaxoSmithKline
Hochgeladen am
4. März 2019
DOI
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Lizenz
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
Beschreibung
Subject diary instruction
Alias
- UMLS CUI-1
- C3890583
- UMLS CUI-2
- C1442085
Beschreibung
This medical research study depends on you filling in this diary EVERY DAY. Thank you for 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 your child took the study medication. It is very important that you report in this diary the dosing information for each day that 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. Should you have any questions about the study medication prior to your next appointment, please contact your study coordinator (see below). Following 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.
Datentyp
text
Alias
- UMLS CUI [1]
- C0337611
Beschreibung
Medication
Alias
- UMLS CUI-1
- C0013227
Beschreibung
Study medication
Datentyp
integer
Alias
- UMLS CUI [1]
- C0013227
Beschreibung
Day of medication
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C0013227
- UMLS CUI [1,2]
- C0439228
Beschreibung
day month year
Datentyp
date
Alias
- UMLS CUI [1,1]
- C0013227
- UMLS CUI [1,2]
- C0011008
Beschreibung
24-hr clock
Datentyp
time
Alias
- UMLS CUI [1,1]
- C0013227
- UMLS CUI [1,2]
- C0040223
- UMLS CUI [1,3]
- C0332170
Beschreibung
24-hr clock
Datentyp
time
Alias
- UMLS CUI [1,1]
- C0013227
- UMLS CUI [1,2]
- C0040223
- UMLS CUI [1,3]
- C0587117
Ähnliche Modelle
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])