Alert Hospital
Addis Ababa, Ethiopia
NCT Number: NCT00919776
Study 2B: Ciclosporin in the management of chronic or recurrent Erythema Nodosum Leprosum Aim: To assess the safety, tolerability and efficacy of Ciclosporin in the treatment of patients whose ENL is not controlled with standard Prednisolone.
Objective: A pilot double blind controlled study randomizing patients whose ENL is not controlled with standard Prednisolone, and comparing a group treated with Ciclosporin to a group treated with additional steroid only.
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Notify Me18 year–65 year
All sexes
Interventional
Phase 2
Addis Ababa, Ethiopia
A pilot double blind controlled study randomizing patients whose ENL is not controlled with standard Prednisolone, and comparing a group treated with Ciclosporin to a group treated with additional steroid only.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
prednisolone 40mg daily then reducing regimen over 16 weeks
Other names: corticosteroids
Ciclosporin 7.5mg/kg - reducing regimen over 16 weeks (additional prednisolone given for the first four weeks)
Other names: Cyclosporine, Cyclosporin A
Time frame: up to 32 weeks
Time frame: up to 32 weeks
Time frame: up to 32 weeks
Time frame: up to 32 weeks
Time frame: up to 32 weeks
Time frame: up to 32 weeks
London School of Hygiene and Tropical Medicine
Other
A Pilot Double Blind Controlled Study Randomizing Patients Whose ENL is Not Controlled With Standard Prednisolone, and Comparing a Group Treated With Ciclosporin to a Group Treated With Additional Steroid Only.
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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