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Children with ALL: Toxicity and Quality of Life Outcomes during Induction Chemotherapy

Toxicity profile during induction chemotherapy and its impact on Quality of Life and treatment outcome in children with Acute Lymphoblastic Leukemia - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2023/08/055970
Enrollment
60
Registered
2023-08-01
Start date
Unknown
Completion date
Unknown
Last updated
2023-08-21

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

Intervention1: NIL: NIL

Sponsors

Dr Antara Sanyal
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Newly diagnosed case of acute lymphoblastic leukemia 2. Age 1-18 years 3. Treatment naïve 4. Diagnosis will be based upon the morphology and immunophenotype of the bone marrow aspirate/ peripheral blood sample

Exclusion criteria

Exclusion criteria: 1. ALL 18 years 2. Relapsed ALL, partially treated ALL 3. Burkittâ??s Leukemia 4. HIV, Hepatitis-B or Hepatitis-C positive cases

Design outcomes

Primary

MeasureTime frame
To assess the Grade three & Grade four toxicity during ALL induction chemotherapyTimepoint: Days 1 to 7 Days 8 to 14 Days 15 to 25 Days 26 to 35

Secondary

MeasureTime frame
1. To assess the quality of life at baseline & at the end of induction using the tool PedsQLâ?¢ 4.0 Generic Core (PedsQL-G) & PedsQLâ?¢ 3.0 Cancer Module (PedsQL-C); 2. To correlate QoL to toxicity during induction treatment; 3. To correlate post induction minimal residual disease (MRD) with baseline clinical characteristics & induction toxicities. Timepoint: At the beginning & end of induction chemotherapy

Countries

India

Contacts

Public ContactDr Antara Sanyal

Institute of Medical Sciences and SUM Hospital, SOA

ssp_scb@yahoo.com8895370579

Outcome results

None listed

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