CompletedPhase 4NCT01975051

A Study to Explore Association of Treatment Regimens for Visceral Leishmaniasis, Host Immunological, Genetical and Nutrition Factors With Post-kala-azar Dermal Leishmaniasis (PKDL)

Studying Leishmaniasis

Last synced from ClinicalTrials.gov

ℹ
Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing data

Key facts

Sponsor
International Centre for Diarrhoeal Disease Research, Bangladesh
Principal Investigator
Dinesh Mondal, MB; MD; PhD
International Centre for Diarrhoeal Disease Research, Bangladesh
Intervention
Mitefosine(drug)
Enrollment
36 enrolled
Eligibility
18-60 years · All sexes
Timeline
2013 – 2014

Study locations (1)

Collaborators

University of Nagasaki.

Primary source

Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.

Open NCT01975051 on ClinicalTrials.gov

Other trials for Leishmaniasis

Additional recruiting or active studies for the same condition.

See all trials for Leishmaniasis →

← Back to all trials