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Prescription and Adverse drug effects analysis in Paediatric Acute Lymphoid Leukaemia .

An Observational Study for Evaluating Prescription Pattern of drugs, Adverse drug reactions in Paediatric Acute Lymphoid Leukaemia in a tertiary care Hospital.

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2021/09/036279
Enrollment
400
Registered
2021-09-07
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: C910- Acute lymphoblastic leukemia [ALL]

Interventions

None listed

Sponsors

Dr Gaurav Narula Professor Medical Oncology Pediatrics Unit
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: a) Patients of either gender and age between 1-15 years treated with one cycle in induction phase (On going or completed consolidation and maintenance phase also included). b) Parent/Legally Acceptable Representative (LAR) of the patient willing to give voluntary informed consent. c) Patient above 8 years willing to give voluntary assent

Exclusion criteria

Exclusion criteria: 1. Any other medical condition, which in the opinion of the investigator precludes the inclusion of the participant. 2. Critically ill patients of Acute lymphoblastic Leukaemia admitted to emergency department 3. Newly diagnosed and treatment naïve patients.

Design outcomes

Primary

MeasureTime frame
Drugs prescribed in treatment of Acute Lymphoblastic Leukaemia patientsTimepoint: 18 months

Secondary

MeasureTime frame
The type, causality, severity and preventability of ADRs in Acute Lymphoblastic Leukaemia. Timepoint: 18 months;To evaluate the Cost of Illness in Acute Lymphoblastic Leukaemia. Timepoint: 18 months

Countries

India

Contacts

Public ContactDr Ankita Kulkarni

Seth GSMC & KEMH Mumbai

yashashrirajit@gmail.com9869193041

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026