Skip to content

Evaluation of protein supplement consumption on the body composition of Hematopoietic Stem Cell Transplantation patients

Evaluation of protein supplementation in body composition and clinical outcome of Hematopoietic Stem Cell Transplantation patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-5kx6drp
Enrollment
Unknown
Registered
2023-07-09
Start date
2022-05-01
Completion date
Unknown
Last updated
2025-10-27

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

Conditions

Hematopoietic Stem Cell Transplantation

Interventions

Randomized, double-blind, controlled, longitudinal, prospective, interventional clinical trial. Whey protein group: 15 patients receive whey protein supplementation (whey protein) in the amount of 1g
G07.203.300.456

Sponsors

Hospital das Clínicas da Faculdade de Medicina de Ribeirão Preto
Lead Sponsor
Fundação Pio XII
Collaborator

Eligibility

Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Age greater than or equal to 18 years; both genders; diagnosis of hematological neoplasms; with indication of the first allogeneic stem cell transplantation

Exclusion criteria

Exclusion criteria: Acute kidney injury; chronic kidney disease

Design outcomes

Primary

MeasureTime frame
Expected outcome: with the use of whey protein supplementation plus leucine will promote muscle mass recovery during allogeneic hematopoietic stem cell transplantation, measured from anthropometric assessment, functionality assessment, body composition assessment and biochemical tests. Data are collected in the preconditioning period, on the day of hematopoietic stem cell infusion, 21 days after infusion, and 100 days after infusion.

Secondary

MeasureTime frame
Expected outcome: the use of whey protein supplementation plus leucine will promote positive nitrogen balance during allogeneic hematopoietic stem cell transplantation, measured from the assessment of nitrogen balance. Data are collected in the preconditioning period, on the day of hematopoietic stem cell infusion, 21 days after infusion, and 100 days after infusion.

Countries

Brazil

Contacts

Public ContactIsabela Schiavoni

Hospital das Clínicas da Faculdade de Medicina de Ribeirão Preto

isabela.schiavoni@usp.br+55 (16) 99601 4543

Outcome results

None listed

Source: REBEC (via WHO ICTRP)