A Randomized Controlled Double Blind Trial of Ciclosporin versus Prednisolone in the Management of Leprosy Patients with New Type 1 Reaction in Ethiopia

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http://eprints.org/relation/isVersionOf https://datacompass.lshtm.ac.uk/id/document/504 http://eprints.org/relation/isVolatileVersionOf https://datacompass.lshtm.ac.uk/id/document/504 http://eprints.org/relation/issmallThumbnailVersionOf https://datacompass.lshtm.ac.uk/id/document/504 indefinite Thumbnails conversion from Text to thumbnail_small archive 38 disk0/00/00/00/91 2015-11-11 14:05:57 2024-03-08 16:50:39 2015-11-11 14:05:57 data_collection show Lambert Saba 0000-0003-4376-5495 TRUE 3fd594932b28b96c66c9e19cc2e7d32f DataManager Nicholls Peter FALSE DataManager Yamuah Laurence FALSE ProjectLeader Lockwood Diana TRUE DataCollector Tsegaye Digafe FALSE DataCollector Nigusse Shimelis FALSE London School of Hygiene & Tropical Medicine, London, United Kingdom A Randomized Controlled Double Blind Trial of Ciclosporin versus Prednisolone in the Management of Leprosy Patients with New Type 1 Reaction in Ethiopia ITCR Leprosy Leprosy reaction Type 1 reaction Adverse events Ciclosporin Prednisolone Data produced as part of a randomized controlled trial to investigate the efficacy and adverse effect profile of ciclosporin in comparison to prednisolone in patients with acute first time occurrence of T1R. Patients were randomized to one of two study arms (ciclosporin treatment or prednisolone treatment) and followed over a 32 week period to assess them for changes in clinical signs and adverse events. 2015-10-01 completed London School of Hygiene & Tropical Medicine 10.17037/DATA.18 Dataset London School of Hygiene & Tropical Medicine, London, United Kingdom MeasurementsAndTests restricted London, United Kingdom Hospital and Homes of St Giles Assessing Ciclosporin in the Treatment of Leprosy Reactions: Evidence from a Randomized Controlled Trial and Other Studies Dataset Quantitative Data from each assessment was recorded on standardised Patient Record Forms (PRF) and kept in a set of case notes separate from other hospital record. Data was verified and entered into Case Record Forms (CRF) by the study physicians. Double data entry into a Microsoft Access 2007 database was performed by Saba Lambera and a data manager at ALERT/AHRI. The double entry was then verified using Epi-Info 3.5.4, with an initial rate of detected errors being under 10%. Errors in the data were verified and corrected in Ethiopia. Errors were traced back to the CRFs and correct. Epi-info was re-run and procedures repeated until two identical and correct databases were obtained. The MS Access data tables were subsequently transferred to SPSS v20 for analysis. ITCRBY24 9.02783 38.847 8.91897 38.6963 en 2011-08-12 2013-07-24 Assessing Ciclosporin in the Treatment of Leprosy Reactions: Evidence from a Randomized Controlled Trial and Other Studies. http://researchonline.lshtm.ac.uk/id/eprint/2021053 Assessing Ciclosporin in the Treatment of Leprosy Reactions: Evidence from a Randomized Controlled Trial and Other Studies Hospital and Homes of St Giles ITCRBY24 ITCRBY24 2015-10-01