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A study to assess the usefulness of various tests done for the monitoring of long term complications in survivors of leukemia and lymphoma.

A prospective observational cohort study to identify the utility of risk-based screening strategy for long term complications in adolescent and adult cancer survivors of leukemia and lymphoma. - LTFU

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2019/06/019880
Enrollment
500
Registered
2019-06-26
Start date
Unknown
Completion date
Unknown
Last updated
2025-11-17

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

Conditions

Health Condition 1: C950- Acute leukemia of unspecified celltype Health Condition 2: C910- Acute lymphoblastic leukemia [ALL] Health Condition 3: C930- Acute monoblastic/monocytic leukemia Health Condition 4: C920- Acute myeloblastic leukemia Health Condition 5: C926- Acute myeloid leukemia with 11q23-abnormality Health Condition 6: C92A- Acute myeloid leukemia with multilineage dysplasia Health Condition 7: C865- Angioimmunoblastic T-cell lymphoma Health Condition 8: C911- Chronic lymphocytic l

Interventions

Intervention1: NIL: NIL Control Intervention1: NIL: NIL

Sponsors

Tata Memorial Centre Research Administrative council
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients previously treated for acute leukemia and lymphoma that are in complete remission. 2. Age more than or equal to 15 years at the time of inclusion into the study. 3. Those that have completed at least 2 years since their last therapy. 4. Willing to follow up at Tata Memorial Center, Mumbai.

Exclusion criteria

Exclusion criteria: Those that have undergone or are planned for hematopoietic stem cell transplant.

Design outcomes

Primary

MeasureTime frame
Proportion of patients who test positive for any of the screening tests throughout the duration of follow up will be estimated.Timepoint: 12 months, 24 months, 36 months

Secondary

MeasureTime frame
1.Yield of a subset of the twenty one diagnostic tests 2. Prevalence of a complication 3. To identify clinical and demographic factors associated with “high yield ? tests. Timepoint: 12 months, 24 months, 36 months

Countries

India

Contacts

Public ContactDr Hasmukh Jain

Tata Memorial Centre

dr.hkjain@gmail.com02224177018

Outcome results

None listed

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