Skip to content

Effect of a Nutritional Formula Composed of Proteins and Carbohydrates on Gastric Emptying in Elderly Individuals

Effect of a Nutritional Formula Composed of Proteins and Carbohydrates on Gastric Emptying in Elderly Individuals: a Randomized, Crossover, Triple-blind Clinical Trial.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07296692
Enrollment
25
Registered
2025-12-22
Start date
2026-02-21
Completion date
2027-05-01
Last updated
2026-05-05

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

Conditions

Gastric Emptying

Keywords

proteíns, elderly, gastric emptying, scintigraphy

Brief summary

The objective of this clinical trial is to evaluate the effect of a nutritional formula composed of carbohydrates and proteins on gastric emptying in elderly individuals aged between 60 and 90 years. The main questions this study aims to answer are: * Does the nutritional formula composed of carbohydrates and proteins delay gastric emptying when compared to a formula composed only of carbohydrates? * Does the formula composed of carbohydrates and proteins cause gastrointestinal symptoms in the study population? The researchers will compare both formulas (carbohydrates and proteins vs. carbohydrates only) to answer the main question. Participants will be required to: * Attend the Nuclear Medicine Department after an 8-hour fast, on two separate days with a minimum interval of seven days for scintigraphy procedures. * Consume the offered formula in a randomized and blinded manner. * Report any gastrointestinal symptoms and complete visual analog scales for sensations such as hunger, satiety, and desire to eat.

Detailed description

Preoperative fasting (POF) is defined as the absence of food or fluid intake in the hours preceding surgery. POF is recommended to minimize the risk of aspiration of gastric contents and related complications. However, the incidence of such complications is low. Prolonged fasting can have adverse effects on the patient's health, such as headache, dehydration, hypovolemia, and hypoglycemia, potentially compromising postoperative recovery. Shortening the fasting period with nutrient-containing clear liquids administered up to two hours before surgery has been shown to be a safe and beneficial alternative. Additionally, the use of formulas containing not only carbohydrates but also proteins has been tested in order to promote further benefits, such as attenuation of negative nitrogen balance and improvement in patient prognosis. Given the increasing life expectancy of the population, the number of surgeries in elderly patients is also growing. This is coupled with the fact that aging is associated with physiological reductions in gastric emptying rate and hydrochloric acid secretion, requiring greater care in determining appropriate POF duration. In this context, the objective of this study is to compare the gastric emptying (GE) of elderly volunteers after consuming a standard formula containing only carbohydrates with another formula composed of both carbohydrates and proteins, administered at two different time points. This is a randomized, crossover, triple-blind clinical trial involving elderly individuals. The study will include individuals aged 60 years or older, who are non-smokers and have no prior diagnosis of conditions that affect gastric emptying. Patients will be randomized into group A or B to determine the order of interventions. Each volunteer will receive the designated formula in a randomized and blinded manner on the study day, with the formula containing approximately 1 mCi of 99mTc-sodium phytate. Immediately after finishing the formula intake, participants will undergo the first scintigraphic imaging (T0). Additional scintigraphic images will be taken at 60, 120, and 180 minutes post-ingestion. The mean time to empty half of the gastric content will be assessed, with values less than 25 minutes considered normal. Gastrointestinal symptoms, as well as sensations of hunger, satiety, and desire to eat, will also be assessed using visual analog scales (VAS), applied on study days. Capillary blood glucose will be measured using a portable glucometer. Data will be analyzed using statistical software, and normality will be tested to determine the appropriate statistical tests. P-values ≥ 0.05 will be considered statistically significant. The sample size will be calculated based on a pilot study involving at least 25 volunteers, since there are no similar prior studies. The parameters from this pilot study may then be used to determine the final sample size.

Interventions

DIETARY_SUPPLEMENTNutren Fresh

In this intervention, participants will receive 200 ml of the nutritional formula.

DIETARY_SUPPLEMENTMaltodextrin (Placebo)

In this intervention, participants will receive 200 ml of maltodextrin.

Sponsors

Federal University of Minas Gerais
Lead SponsorOTHER
Nestle Health Science
CollaboratorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
SUPPORTIVE_CARE
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
60 Years to 90 Years
Healthy volunteers
Yes

Inclusion criteria

* Elderly individuals aged between 60 and 90 years * Non-smokers * No prior diagnosis of conditions that affect gastric emptying, such as: * Gastroesophageal reflux * Gastroparesis * Untreated Helicobacter pylori (H. pylori) infection * Stomach cancer * Esophageal cancer

Exclusion criteria

* Volunteers who do not meet the inclusion criteria * Refusal to sign the informed consent form (ICF) * Volunteers with obesity (BMI over 35 kg/m²) * Volunteers who do not eat orally or have a prior diagnosis of delayed gastric emptying and are on routine use of prokinetic medications * Individuals diagnosed with Alzheimer's or Parkinson's disease

Design outcomes

Primary

MeasureTime frameDescription
Gastric EmptyingOn day 1 and day 2 of the protocol.Gastric emptying will be assessed through scintigraphic imaging obtained immediately after formula consumption and every hour for three hours.

Secondary

MeasureTime frameDescription
Gastrointestinal symptoms and sensations of hungry, saciety and desire to eatImmediately after formula ingestion, and at 60, 120, and 180 minutes post-ingestion.Use of numerical visual analog scales (from 0 to 10, with 0 indicating no symptoms and 10 indicating severe symptoms.), where the volunteer will indicate the presence and intensity of gastrointestinal symptoms (heartburn, nausea, burning sensation, etc.) and sensations of hunger, satiety, and desire to eat.
Blood glucoseThis assessment will be conducted with the patient in a fasting state, immediately after formula ingestion, and at 60, 120, and 180 minutes post-ingestion on each protocol day.To assess capillary blood glucose using a portable glucometer.

Countries

Brazil

Contacts

CONTACTSimone de Vasconcelos Generoso Generoso, Phd
simonenutufmg@gmail.com55(031) 988128650
PRINCIPAL_INVESTIGATORSimone de Vasconcelos Generoso Generoso, Phd

Department of Nutrition, Federal University of Minas Gerais

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 6, 2026