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KETO-TUMOR: a Study on Brain Tumors and Central Obesity

Single-arm, Open-label, Single-center, Non-profit Interventional Clinical Trial on the Effects of the Ketogenic Diet in Patients With Brain Tumors and Central Obesity

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07396896
Enrollment
30
Registered
2026-02-09
Start date
2025-05-08
Completion date
2028-04-01
Last updated
2026-02-09

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

Conditions

Hypothalamic Neoplasms, Obese Patients

Brief summary

Hypothalamic-chiasmatic tumours account for 5-10% of CNS tumours in children and can compromise hypothalamic function, causing alterations in energy balance and weight gain. In inoperable cases, chemotherapy and radiotherapy are used; the latter, although the gold standard, is associated with significant neurocognitive and endocrine-metabolic side effects, proportional to the hypothalamic damage. The ketogenic diet, used for decades in the treatment of drug-resistant childhood epilepsy, induces the use of ketone bodies as a source of energy for the brain and is effective in controlling seizures. Among the different variants, the modified Atkins diet was chosen in this study to promote better patient adherence. This study aims to evaluate the effectiveness of the ketogenic diet (KD) in treating central obesity secondary to hypothalamic-chiasmatic tumours (gliomas, craniopharyngiomas, germ cell tumours, etc.), which often lead to excessive weight gain. This is refractory to drug therapy and lifestyle changes, such as low-calorie diets and exercise.

Interventions

BEHAVIORALDietary intervention

Atkins Modified Diet (MAD)

Sponsors

Meyer Children's Hospital IRCCS
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
7 Years to 30 Years
Healthy volunteers
No

Inclusion criteria

1. Diagnosis of hypothalamic-chiasmatic tumour according to the WHO 2021 classification 2. Diagnosis of hypothalamic obesity: after 5 years of age, BMI \>97th percentile in the WHO 2007 curves 3. Males and females aged between 7 and 30 years 4. Performance status: Lansky score \> 40 for patients aged \< 18 years and Karnofsky score \> 40 for patients aged between 18 and 30 years 5. Signature of informed consent to participate in the study 6. Signature of consent by the minor patient to participate in the study (7-13 years and 14-17 years).

Exclusion criteria

1\. Deficiencies of: * Primary carnitine * Carnitine palmitoyltransferase 2 (CPT 2) * Carnitine acylcarnitine translocase (CACT) * Beta-oxidation * Medium-chain acyl-CoA dehydrogenase (MCAD) * long-chain acyl-CoA dehydrogenase (LCAD) * short-chain acyl-CoA dehydrogenase (SCAD) * porphyria * pyruvate carboxylase * long-chain 3-hydroxyacyl-CoA dehydrogenase.

Design outcomes

Primary

MeasureTime frame
Percentage of patients who experience weight loss of at least 5% over 24 monthsFrom enrollment to the end of the follow up period at 24 months

Secondary

MeasureTime frame
Percentage of patients showing weight reduction, improvement in lipid and carbohydrate parametersFrom enrollment to the end of the follow up period at 24 months
Percentage of patients with ketosisFrom enrollement to the end of the follow up period at 24 months
Percentage of patients with serious adverse eventsFrom enrollement to the end of the follow up period at 24 months
Adherence rate to the proposed dietary intervention, considering the number of patients who discontinue the diet and those who continue itFrom enrollment to the end of the follow up at 24 months
Percentage of patients showing reduction of lean body mass in 24 monthsFrom enrollment to the end of the follow up period at 24 months

Countries

Italy

Contacts

CONTACTIacopo Sardi
iacopo.sardi@meyer.it0555662631

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 10, 2026