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A study to develop a software for predicting the outcomes of febrile neutropenia (FN) in adolescent and adults with blood cancers

A study to develop an artificial intelligence algorithm for predicting the outcomes of febrile neutropenia (FN) in adolescent and adults with hematological malignancies - AI FN

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2021/11/037855
Enrollment
500
Registered
2021-11-08
Start date
Unknown
Completion date
Unknown
Last updated
2022-02-21

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

Conditions

Health Condition 1: C969- Malignant neoplasm of lymphoid, hematopoietic and related tissue, unspecified

Interventions

None listed

Sponsors

Tata Memorial Hospital Research Administrative Council
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients with leukemia, lymphoma and myeloma on chemotherapy. 2. Age more than or equal to 15 years. 3. Patients with Febrile Neutropenia

Exclusion criteria

Exclusion criteria: None

Design outcomes

Primary

MeasureTime frame
To predict the complications in high risk FN patients complication being defined as need for intensive care admission, need for mechanical ventilation, need for vasopressor support, renal failure, arrhythmias requiring treatment, confused/altered mental state, congestive cardiac failure, bleeding requiring transfusion or death. Timepoint: This will be studied till day 28 from the day of onset of the episode

Secondary

MeasureTime frame
The probability of isolating a drug resistant organism based on clinical, laboratory and hospital antibiogram at the baseline will be assessed.Timepoint: At the baseline;To predict the complications in low risk FN patients complication being defined as need for intensive care admission, need for mechanical ventilation, need for vasopressor support, renal failure, arrhythmias requiring treatment, confused/altered mental state, congestive cardiac failure, bleeding requiring transfusion or death.Timepoint: This will be studied till day 28 from the day of onset of the episode

Countries

India

Contacts

Public ContactDr Hemanth Muthuluri

Tata Memorial Hospital

drhemanth88@gmail.com9491538357

Outcome results

None listed

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