ID
35595
Beschrijving
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 concomitant medication form. The concomitant medication has to be filled in if the subject used concomitant medications during study.
Link
https://clinicaltrials.gov/ct2/show/NCT00852540
Trefwoorden
Versies (3)
- 04-03-19 04-03-19 -
- 04-03-19 04-03-19 -
- 11-03-19 11-03-19 -
Houder van rechten
GlaxoSmithKline
Geüploaded op
11 maart 2019
DOI
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Licentie
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
Concomitant medication
- StudyEvent: ODM
Beschrijving
Prior medications
Alias
- UMLS CUI-1
- C2347852
Beschrijving
(Trade Name preferred)
Datatype
text
Alias
- UMLS CUI [1]
- C0013227
Beschrijving
Total Daily Dose
Datatype
text
Alias
- UMLS CUI [1,1]
- C2348070
- UMLS CUI [1,2]
- C0013227
Beschrijving
Units
Datatype
integer
Alias
- UMLS CUI [1]
- C1519795
Beschrijving
Route
Datatype
integer
Alias
- UMLS CUI [1]
- C0013153
Beschrijving
Reason for Medication
Datatype
text
Alias
- UMLS CUI [1]
- C2826696
Beschrijving
day month year
Datatype
date
Alias
- UMLS CUI [1,1]
- C0013227
- UMLS CUI [1,2]
- C0808070
Beschrijving
Taken prior to study
Datatype
text
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C0332152
- UMLS CUI [1,3]
- C2347804
Beschrijving
Medication ongoing
Datatype
text
Alias
- UMLS CUI [1]
- C2826666
Beschrijving
day month year
Datatype
date
Alias
- UMLS CUI [1,1]
- C0013227
- UMLS CUI [1,2]
- C0806020
Similar models
Concomitant medication
- StudyEvent: ODM
C0013227 (UMLS CUI [1,2])
C0808070 (UMLS CUI [1,2])
C0332152 (UMLS CUI [1,2])
C2347804 (UMLS CUI [1,3])
C0806020 (UMLS CUI [1,2])