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NCT04764695Completed

Body Composition and Nutritional Status in Pediatric Patients With Hematological Malignancies

Evaluation of Body Composition and Nutritional Status in Pediatric Patients With Hematological Malignancies

Source: ClinicalTrials.gov · Last updated 6 Dec 2024

Brief summary (registry, in English)

Introduction: Annually 400,000 children are diagnosed with cancer in the world. Approximately 90% live in low/middle-income countries, with survival rates of 10-30%. In Mexico, children and adolescents' hospital admissions for cancer are mainly leukemias (46%), being acute lymphoblastic leukemia (ALL) the most common. Half of ALL patients have an altered nutritional status at the time of diagnosis. Nutritional assessment is performed using conventional anthropometric measures, which are not sensitive to changes in fat-free mass and fat mass (FFM and FFM). Our objective is to evaluate the body composition and nutritional status in pediatric patients with HM. This is a pre-test/post-test clinical trial. Children 2-14 y olds diagnosed with leukemia, myeloma and lymphoma in any stage of oncological treatment will participate. The nutritional status will be evaluated using questionnaires and body composition. Measurements will occur at the enrrollment of the study and 6 months after.

Status (registry)
Completed
Study type
Interventional
Enrollment
38 (actual)
First submitted
10 Feb 2021
Start date
Jan 2023
Primary completion date
Aug 2024
Lead sponsor
Universidad de Sonora
NCT number
NCT04764695

What you commit to

  • Study type: Interventional
  • Participants enrolled: 38
  • From Jan 2023 to the primary completion date, Aug 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Pathological conditions that can alter body composition (diabetes, hypothyroidism, among others)

Other

  • Patients with sepsis that causes hemodynamic compromise and cannot be evaluated
  • Severely ill patients unable to participate in baseline measurements
  • Relapsed patients
  • Patients with developmental problems of a genetic order as well as innate errors of metabolism

Who the study is looking for

  • Patients in remission stage (4 - 6 weeks)
  • Life expectancy\> 6 months and sufficient general conditions according to scales (Lansky ≥ 50 points for children \<16 years)
  • Histopathological/molecular clinical confirmation of the HM diagnosis
  • Signature of the consent by the relative or legal guardian of the patient and as well as the consent informed by the patient.

Age in the registry: 2 years to 14 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Universidad de Sonora
Coordinator of this site? Confirm its status
HermosilloMexicoUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.