Treatment Protocol for Clofazamine in the Long Term Treatment of Leprosy
NCT ID: NCT00852345
Last Updated: 2015-04-03
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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Brief Summary
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Detailed Description
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Conditions
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Interventions
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clofazamine
clofazamine 50mg po qday (duration varies according to physician)
Eligibility Criteria
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Inclusion Criteria
* Multibacillary leprosy (lepromatous leprosy or borderline-lepromatous).
* Paucibacillary leprosy (borderline, borderline tuberculoid, or indeterminate) if there is involvement of the cranial nerves or active acute neuritis.
* Known or suspected ENL(erythema nodosum leprosum) (a specific immune reaction with painful skin nodules and fever)
* Known or suspected dapsone-resistant leprosy or relapsed leprosy.
* Intolerance of other antileprosy antibiotic (where clofazamine is substituted as apart of multidrug regimen)
Exclusion Criteria
* Known prior intolerance of Clofazamine
* Any minor (even with parental consent)
* Any fertile woman who is pregnant a specific immune reaction with painful skin rash and fever)
18 Years
ALL
No
Sponsors
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Health Resources and Services Administration (HRSA)
FED
Kaiser Permanente
OTHER
Responsible Party
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Principal Investigators
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Arnold M Henson, MD
Role: PRINCIPAL_INVESTIGATOR
Kaiser Permanente
Locations
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Kaiser Permanente
Irvine, California, United States
Countries
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Other Identifiers
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KPSC IRB 5347
Identifier Type: OTHER
Identifier Source: secondary_id
IRB 5347
Identifier Type: -
Identifier Source: org_study_id
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