None listed
Conditions
Interventions
Intervention1: It is an observational study, no intervention will be done:
Control Intervention1: It is an observational study, no intervention will be done:
Sponsors
Dr. KH Reeta,
Assistant professor
Department of Pharmacology
AIIMS, New Delhi-110029
Department of Pharmacology,
AIIMS, New Delhi
PROF YK GUPTA
Eligibility
Inclusion criteria
Inclusion criteria: Patients of acute myeloid leukemia of either sex in the age ≤ 60 years who are willing for treatment.
Exclusion criteria
Exclusion criteria: (1) Patients with aleukemic leukemia. (2) Patients with AML M3 sub type. (3) Patients with contraindication for chemotherapy. (4) Patients not willing for the treatment. (5) Patients not giving written consent for the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Correlation between the results of in vitro study and outcome of induction chemotherapy in terms of complete remission achieved or not.Timepoint: Baseline and at 21-28 days after induction chemotherapy | — |
Secondary
| Measure | Time frame |
|---|---|
| To see if there is any difference in the study results from bone marrow samples and peripheral blood samples.Timepoint: 21-28 days after induction chemotherapy | — |
Countries
India
Contacts
Public ContactDR HEMANT SINGH BHADAURIA
All India Institute of Medical Sciences
Outcome results
None listed