Tundra Space

Tundra Space

Clinical Research Directory

Browse clinical research sites, groups, and studies.

Back to Studies
RECRUITING
NCT07675421
NA

Impact of HMB Supplementation on Inflammation and Outcomes in Head and Neck Cancer

Sponsor: Federal University of Minas Gerais

View on ClinicalTrials.gov

Summary

Cancer patients undergoing surgery are at high risk of malnutrition due to the effects of the tumor and surgical stress, which can lead to worse clinical outcomes. This study aims to evaluate the impact of beta-hydroxy-beta-methylbutyrate (HMB) supplementation on inflammatory markers and clinical outcomes in patients with malignant tumors of the upper airways and digestive tract undergoing surgery. This is a randomized, double-blind clinical trial. Participants will be randomly assigned to one of two groups: intervention (3 g/day of HMB) or control (3 g/day of maltodextrin) for 30 days prior to surgery. Initial assessments will include nutritional status, muscle strength, quadriceps muscle thickness by ultrasound, and laboratory tests. Postoperative clinical outcomes will be monitored through electronic medical records.

Official title: Impact of Beta Hydroxy Methyl Butyrate (HMB) Supplementation on Inflammatory Markers and Clinical Outcomes in Patients With Head And Neck Cancer

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

66

Start Date

2026-08-01

Completion Date

2027-11-30

Last Updated

2026-06-30

Healthy Volunteers

No

Interventions

DIETARY_SUPPLEMENT

HMB, hydroxymethylbutyrate

Participants will receive one sachet per day containing 3 g of β-hydroxy β-methylbutyrate (HMB) for 30 days prior to surgery.

DIETARY_SUPPLEMENT

Maltodextrin (Placebo)

Participants will receive one sachet per day containing 3 g of maltodextrin (placebo) for 30 days prior to surgery.

Locations (1)

School of Medicine, Federal University of Minas Gerais

Belo Horizonte, Minas Gerais, Brazil