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Trials / Completed

CompletedNCT00310505

Amphotericin B Treatment in Visceral Leishmaniasis

Randomised Double Blind Dose Ranging Study of Amphotericin B in Visceral Leishmaniasis

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
1,500 (planned)
Sponsor
Banaras Hindu University · Academic / Other
Sex
All
Age
2 Years – 65 Years
Healthy volunteers
Not accepted

Summary

This study is being conducted to assess the safety and efficacy of amphotericin B deoxycholate in doses of 0.75 mg/kg or 1.0 mg/kg for 15 doses. In each arm the drug is given in the conventional way every alternate day against the daily administration regimen being tested.

Detailed description

This study is being conducted to assess the safety and efficacy of amphotericin B deoxycholate in doses of 0.75 mg/kg or 1.0 mg/kg for 15 doses. In each arm the drug is given in the conventional way every alternate day against the daily administration regimen being tested.

Conditions

Interventions

TypeNameDescription
DRUGAmphotericin B deoxycholate given as daily administration

Timeline

Start date
2003-01-01
First posted
2006-04-04
Last updated
2008-09-12

Locations

1 site across 1 country: India

Source: ClinicalTrials.gov record NCT00310505. Inclusion in this directory is not an endorsement.

Amphotericin B Treatment in Visceral Leishmaniasis (NCT00310505) · Clinical Trials Directory