Ciclosporin in the management of ENL reactions

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http://eprints.org/relation/isVersionOf https://datacompass.lshtm.ac.uk/id/document/489 http://eprints.org/relation/isVolatileVersionOf https://datacompass.lshtm.ac.uk/id/document/489 http://eprints.org/relation/isIndexCodesVersionOf https://datacompass.lshtm.ac.uk/id/document/489 indefinite Generate index codes conversion from Text to indexcodes archive 38 disk0/00/00/00/90 2015-11-11 14:04:52 2022-04-27 18:19:42 2015-11-11 14:04:52 data_collection show Lambert Saba 0000-0003-4376-5495 TRUE 3fd594932b28b96c66c9e19cc2e7d32f DataManager Nicholls Peter FALSE Yamuah Laurence FALSE Lockwood Diana TRUE ProjectLeader Tsegaye Digafe FALSE Nigusse Shimelis FALSE London School of Hygiene & Tropical Medicine, London, United Kingdom Ciclosporin in the management of ENL reactions PHSE Leprosy Leprosy reaction Erythema Nodosum Leprosum Adverse events Ciclosporin Prednisolone Data produced as part of a clinical trial to compare the efficacy and safety of Ciclosporin and Prednisolone in the Treatment of Erythema Nodosum Leprosum (ENL). The trial was conducted with two randomised, double blind, controlled groups in Ethiopia. The first group had acute first time occurrence of ENL and the second group had recurrent ENL. Both groups were randomized to one of two study arms: the ciclosporin treatment arm or the prednisolone treatment arm. Patients were followed over a 32 week period, where they were assessed for changes in clinical signs and adverse events. 2015-10-01 completed London School of Hygiene & Tropical Medicine 10.17037/DATA.17 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. Double entry was then verified using Epi-Info 3.5.4. The initial rate of errors detected by double entry was just 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. Finally, the MS Access data tables were transferred to SPSS v20 for analysis. ITCRBY24 9.06403 38.8541 8.90533 38.6321 en 2011-08-12 2012-05-10 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