Evaluation of the Cardioprotective Effect of L-carnitine and Silymarin in Patients Receiving Anthracycline Chemotherapy

PHASE4CompletedINTERVENTIONAL
Enrollment

83

Participants

Timeline

Start Date

September 10, 2018

Primary Completion Date

August 13, 2019

Study Completion Date

December 10, 2019

Conditions
Breast Cancer
Interventions
DRUG

L-Carnitine 500Mg Oral Tablet

"eighty-three eligible patients were recruited 33, 25, and 25 patients in the control group, L-carnitine group, and, Silymarin group respectively, completed the study~without cardioprotective agents in a dose of 50 mg/m2. L-carnitine group received anthracycline-containing chemotherapy in a dose of 50 mg/m2 plus L-carnitine 3 gm L-carnitine® capsules obtained from (MEPACO) was taken PO one day before chemotherapeutic cycle and 1gm /day during the following 21 days. Silymarin group received anthracycline-containing chemotherapy in a dose of 50 mg/m2 plus Silymarin as cardioprotective agent.140 mg (Legalon ® 140 mg capsule obtained from (MEDA). Silymarin was taken PO once daily after meals during the chemotherapeutic cycle. The treatment period was 6 months."

Trial Locations (1)

34518

Horus University, Damietta

All Listed Sponsors
lead

Horus University

OTHER

NCT04434404 - Evaluation of the Cardioprotective Effect of L-carnitine and Silymarin in Patients Receiving Anthracycline Chemotherapy | Biotech Hunter | Biotech Hunter