ID
35674
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 Clinical diagnosis form. It has to be filled in for screening (Visit 1, Baseline).
Link
https://clinicaltrials.gov/ct2/show/NCT00852540
Palabras clave
Versiones (2)
- 11/3/19 11/3/19 -
- 15/3/19 15/3/19 - Sarah Riepenhausen
Titular de derechos de autor
GlaxoSmithKline
Subido en
15 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
Clinical diagnosis
- StudyEvent: ODM
Descripción
Clinical diagnosis
Alias
- UMLS CUI-1
- C0332140
Descripción
[Other] Medical Conditions
Alias
- UMLS CUI-1
- C0012634
- UMLS CUI-2
- C0205394
Similar models
Clinical diagnosis
- StudyEvent: ODM
C0004623 (UMLS CUI [1,2])
C0205394 (UMLS CUI-2)
C2348235 (UMLS CUI [1,2])