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Amphotericin B Treatment in Visceral Leishmaniasis

B

Banaras Hindu University

Status

Completed

Conditions

Visceral Leishmaniasis

Treatments

Drug: Amphotericin B deoxycholate given as daily administration

Study type

Interventional

Funder types

Other

Identifiers

NCT00310505
SS01MZP03

Details and patient eligibility

About

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.

Full 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.

Sex

All

Ages

2 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Parasitologically proved kala-azar

Exclusion criteria

  • HIV positive serology

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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