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Recruiting Phase 4

Hepatoprotective for Children and Adolescent With Acute Lymphoblastic Leukemia

NCT06918054 · tracked via the Priya Life Science Egypt tracker
Phase
Phase 4
Started
2023-11-17
Last updated
2025-04-09

Condition(s) studied

Leukaemia (Acute)Acute Lymphoblastic Leukemia

Investigational drug(s) / intervention(s)

Dietary modificationSupplementation of omega 3 fatty acids

Dietary modification: Patients will follow Mediterranean Diet (MD), this diet is characterized by a high intake of vegetables, fruit, whole cereals, legumes, nuts, and fish and a low intake of red meat and homemade desserts. The main added fat was extra virgin olive oil, with 35-40% kcal from fat (\<10% from saturated fat), 40-44% kcal from carbohydrate, and 20% kcal from protein

Supplementation of omega 3 fatty acids: Supplementation of omega 3 fatty acids ( dose based on weight: \<40 kg-450 mg/day, 40-60 kg-900 mg/day, \>60 kg-1300 mg/day)

Study summary

This current study will implement a proposed whole program of monitoring and prevention acute hepatic injury during the time of induction chemotherapy in children and adolescent with ALL.

Eligibility

Sex
ALL
Min age
2 Years
Max age
18 Years
Healthy volunteers
Accepted
Inclusion Criteria: Children and adolescents aged from 2 to 18 years newly diagnosed with acute lymphoblastic leukemia during induction phase of chemotherapy treated at Ain Shams Exclusion Criteria: Known chronic liver disease.

Primary outcome measure(s)

  • Implementation a program of hepatic support — Almost 1 year
    To implement a hepatoprotection interventional program to children and adolescent with ALL during Total XV induction c

Trial sites (2)

FacilityCityRegionStatus
Ain Shams University Cairo Egypt Recruiting
Faculty of Medicine Ain Shams Research Institute- Clinical Research Center (MASRI-CRC) Cairo Egypt Recruiting

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06918054 on ClinicalTrials.gov ↗ ← All trials in Egypt