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Transient Elastgraphy fo pediatric patients with acute lymphoblastic leukemia to evaluate liver steatosis

Transient Elastgraphy fo pediatric patients with acute lymphoblastic leukemia to evaluate liver steatosis: the single centre study.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCT1032210047
Enrollment
20
Registered
2021-04-22
Start date
2021-09-27
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

de novo acute lymphoblastic leukemia

Interventions

After enrollment, we will evaluate CAP value using transient elastography to assess steatosis before initiating the treatment for acute lymphoblastic leukemia. CAP value is measured with evaluating ci

Sponsors

Tanoshima Reo
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. De novo pediatric patients (age < 20 years old) who were diagnosed as acute lymphoblastic leukemia, planning to perform chemotherapy in our hospital. 2. Performance status 0-2 3. Patients whose legal gurdians provide written informed consents.

Exclusion criteria

Exclusion criteria: 1. Patients who have chronic hepatitis such as HBV or HCV. 2. Patients who are extremely anxious for the exam. 3. Patients who are allergic to ultrasound gel. 4. Patients whose body mass index are more than 30. 5. Patients who have preivious hisotory of malignant diseases or cancer chemotherapy. 6. Other reasons for inapproate candidates of this study.

Design outcomes

Primary

MeasureTime frame
The proportion of patients whose Controlled Attenuation Parameter (CAP) were above 225 dB/m.

Secondary

MeasureTime frame
To compare of CAP between pretreatment and post-induction therapy. To investigate chronological changes of CAP. To evaluate factors of CAP > 225 dB/, after induction therapy (AST, ALT, total cholesterol, triglyceride)

Contacts

Public ContactReo Tanoshima

Yokohama City University Hospital

reotano@yokohama-cu.ac.jp+81-45-787-2800

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026