CompletedPhase 3NCT00216346

Safety and Efficacy Study of Paromomycin to Treat Visceral Leishmaniasis

Studying Leishmaniasis

Last synced from ClinicalTrials.gov

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

Key facts

Sponsor
PATH
Principal Investigator
Prof S. Sundar
Kala-azar Research Centre
Intervention
Paromomycin sulfate(drug)
Enrollment
667 target
Eligibility
5-55 years · All sexes
Timeline
20032004

Study locations (4)

Collaborators

World Health Organization

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 NCT00216346 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