50
Participants
Start Date
October 10, 2017
Primary Completion Date
July 17, 2018
Study Completion Date
July 17, 2018
Tamoxifen
Tamoxifen will be given orally in a dose of 300mg/day for the first 14 days following randomization. It will be administered by nasogastric tube where patients are unconscious. The Tamoxifen will be administered in the morning combined with amphotericin and fluconazole dose.
Amphotericin B
Patients will receive amphotericin 1mg/kg/day i.v. once daily orally for the first 2 weeks.
Fluconazole
Patients will receive fluconazole 800mg once daily orally for the first 2 weeks. Amphotericin and fluconazole will be administered simultaneously. After the first 2 weeks of study treatment, all patients will receive fluconazole 800mg/day for 8 further weeks, until the study end.
Cho Ray Hospital, Ho Chi Minh City
Hospital for Tropical Diseases, Ho Chi Minh City
Oxford University Clinical Research Unit, Ho Chi Minh City
Hospital for Tropical Diseases, Ho Chi Minh City, Vietnam
OTHER
Cho Ray Hospital
OTHER
University of Liverpool
OTHER
University of Rochester
OTHER
Liverpool School of Tropical Medicine
OTHER
Oxford University Clinical Research Unit, Vietnam
OTHER