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

Status: Recruiting
Location: See location...
Intervention Type: Dietary supplement
Study Type: Interventional
Study Phase: Not Applicable
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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Individuals aged 18 years or older;

• Both sexes (male and female);

• Patients treated at the outpatient clinic for head and neck carcinoma;

• Indication for potentially curative tumor resection surgery.

Locations
Other Locations
Brazil
School of Medicine, Federal University of Minas Gerais
RECRUITING
Belo Horizonte
Contact Information
Primary
Marcus Vinícius M Andrade, MD, PhD
andrademufmg@gmail.com
+55 31 98805-3393
Backup
Simone V Generoso, PhD
simonenutufmg@gmail.com
+55 31 988128650
Time Frame
Start Date: 2026-08-01
Estimated Completion Date: 2027-11-30
Participants
Target number of participants: 66
Treatments
Experimental: HMB group
Participants in the intervention group will receive one sachet per day containing 3 g of β-hydroxy β-methylbutyrate (HMB) for 30 days prior to surgery. The supplementation is intended to support nutritional status, muscle mass preservation, and improve preoperative outcomes.
Placebo_comparator: Control group
Participants in the control group will receive one sachet per day containing 3 g of maltodextrin (placebo) for 30 days prior to surgery. The placebo is identical in appearance and dosage to the intervention supplement but does not contain the active ingredient.
Related Therapeutic Areas
Sponsors
Leads: Federal University of Minas Gerais

This content was sourced from clinicaltrials.gov