Personalized Pharmaconutrition Therapy for Myosteatosis, Sarcopenia, and Prognosis in Gastric Cancer Patients

NCT07466758 | Completed Phase 2 DMC

• 1 other identifier: BİRUNİ-BAP-12-2025-01-51
• Study Type: interventional
• Target: 40
• Locations: 1 country
• Sites: 2

Brief Summary

This randomized controlled trial aims to evaluate the effect of personalized pharmaconutrition therapy on myosteatosis, sarcopenia, and disease prognosis in patients undergoing surgery due to gastric cancer. Myosteatosis refers to the accumulation of fat within skeletal muscle and is an important indicator of muscle quality and may be associated with postoperative recovery and disease outcomes. A total of 40 patients will be included in the study (20 controls, 20 intervention). In addition to standard nutritional care, the intervention group will receive an amino acid-based pharmaconutrition protocol containing glutamine, arginine, and beta-hydroxy-beta-methylbutyrate. The pharmaconutritional intervention will be dosed according to individual requirements so that the total protein intake from the diet is 1-1.5 g/kg, based on the analysis of weekly food consumption records taken from the start to the end of the study. The control group will receive only standard nutritional care. Myosteatosis, an indicator of muscle quality, will be assessed using computed tomography (CT) images obtained at the level of the third lumbar vertebra (L3). For the evaluation of myosteatosis, the mean radiodensity of skeletal muscle within the range of -29 to +150 Hounsfield Units (HU) will be used. Sarcopenia will be determined using the skeletal muscle index (SMI), which is calculated by dividing skeletal muscle area (SMA) by the square of height (cm²/m²). In addition, clinical and nutritional parameters will also be evaluated. Measurements will be performed at one week before surgery and at postoperative week 4. Disease prognosis will be evaluated using the Glasgow Prognostic Score and the Prognostic Nutritional Index. The aim of this study is to determine the effects of personalized pharmaconutrition therapy on myosteatosis, sarcopenia, disease prognosis, and clinical outcomes in patients with gastric cancer. Research Question: Does personalized pharmaconutrition therapy affect myosteatosis and sarcopenia in patients undergoing gastric cancer surgery?

Conditions

Myosteatosis; Sarcopenia

Outcome Measures

Primary Outcomes (1)

• Change in Skeletal Muscle Myosteatosis at the L3 Level Assessed by Computed Tomography

  Myosteatosis will be assessed using computed tomography images at the L3 vertebral level. Skeletal muscle radiodensity (Hounsfield Units) will be used to evaluate myosteatosis. Changes between baseline and week 5 will be assessed in both the intervention and control groups.

  Baseline and Postoperative week 4

Secondary Outcomes (1)

• Change in Skeletal Muscle Index (SMI)

  Baseline and Postoperative week 4

Study Arms (2)

Personalised Pharmaconutrition Group

EXPERIMENTAL

Drug: Pharmaconutrition

Control Group

NO INTERVENTION

Interventions

Pharmaconutrition DRUG

The intervention includes a personalised pharmaconutrition formula containing arginine, glutamine, and beta-hydroxy-beta-methylbutyrate (HMB). It is administered orally as a powder dissolved in water. The intervention is applied for one week before surgery and four weeks after surgery. The dosage is individually adjusted every week based on retrospective 24-hour dietary recall data to ensure total daily protein intake reaches 1.0-1.5 g/kg/day. The product is used as a dietary supplement and does not replace meals.

Personalised Pharmaconutrition Group

Eligibility Criteria

• Age: 18 Years - 65 Years
• Sex: male
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Male adults aged between 18 and 64 years
• Diagnosed with primary or recurrent gastric cancer and eligible for surgery
• Body Mass Index (BMI) within the normal range (18.5-24.9 kg/m²)
• Capable of oral or enteral feeding
• Provided written informed consent

You may not qualify if:

• Absence of written informed consent
• Female sex
• Diagnosis of a benign tumor or a tumor located outside the stomach
• Not requiring surgical intervention
• Presence of renal failure or hepatic failure
• Presence of overt ascites or edema within the past month
• Prior use of the pharmaconutrition product planned for this study

Sponsors & Collaborators

• Biruni University: lead
• Halic University: collaborator

Study Sites (2)

Basaksehir Cam and Sakura City Hospital

Istanbul, Turkey (Türkiye)

Location

Istanbul Haseki Training and Research Hospital

Istanbul, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Sarcopenia

Condition Hierarchy (Ancestors)

Muscular Atrophy; Neuromuscular Manifestations; Neurologic Manifestations; Nervous System Diseases; Atrophy; Pathological Conditions, Anatomical; Pathological Conditions, Signs and Symptoms; Signs and Symptoms

Study Design

• Study Type: interventional
• Phase: phase 2
• Allocation: RANDOMIZED
• Masking: NONE
• Purpose: PREVENTION
• Intervention Model: PARALLEL
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Lecturer

Study Record Dates

• First Submitted: March 4, 2026
• First Posted: March 12, 2026
• Study Start: October 16, 2024
• Primary Completion: March 4, 2026
• Study Completion: March 4, 2026
• Last Updated: March 12, 2026

Record last verified: 2026-03

Data Sharing

• IPD Sharing: Will not share

Locations

TU (2)