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Clinical Trials/NCT07121803
NCT07121803RecruitingNot Applicable

Analysis of Effects of Specialized Food Products Based on Ice-Cream on Esophageal Motility

Federal State Budgetary Scientific Institution "Federal Research Centre of Nutrition, Biotechnology1 site in 1 country30 target enrollmentStarted: July 1, 2025Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Sponsor
Enrollment
30
Locations
1
Primary Endpoint
Mean contractile front velocity

Study Overview

Brief Summary

This study aims to assess the influence of specialized products based on ice cream on esophageal motility

Detailed Description

During this study participants will be examined with the use of high-resolution esophageal motility. After standard procedure, according to Chicago IV protocol, subjects will be provided with 3 different types of food products: standard icecream (sundae), icecream with brazzein, maltitol and oligofructose; icecream with brazzein, erythritol, maltitol and inulin. Tolerability of products will be assessed based on specialized scales and formal questioning.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Crossover
Primary Purpose
Basic Science
Masking
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to 80 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •willingness to participate based on signed written informed consent;
  • •controlled glycemia. If stable glycemia is achieved on treatment, the following requirements should be met:
  • •no qualitative changes in treatment within 6 months before enrollment (i.e., the introduction of a new antidiabetic therapy);
  • •doses of anti-diabetic medications should be stable for 6 month in patients who receive metformin, gliptins, sulfonylureas, sodium/glucose cotransporter 2 (SGLT-2) inhibitors, glucagon-like peptide 1 agonists (GLP-1) or insulin.
  • •no new medications during participation in the study

Exclusion Criteria

  • •Pregnancy and breastfeeding;
  • •Liver cirrhosis based on liver histology, or liver stiffness measurement (LSM > or = 14 kPa by Fibroscan), or APRI > or= 1; or BARD score > or =
  • •Diarrhea of any type (watery stool more than 3 times a day).
  • •Chronic heart failure (I-IV class by NYHA).
  • •Past major abdominal or chest surgery, including bariatric procedures and fundoplication (except appendectomy or cholecystectomy performed more than a year before enrollment).
  • •Achalasia and esophago-gastric junction outflow obstruction
  • •Major esophageal motility disorders according to Chicago IV classification.
  • •Clinically relevant acute cardiovascular event within 6 months prior to screening.
  • •Uncontrolled arterial hypertension despite optimal anti-hypertensive therapy.
  • •Diabetes mellitus type
  • •The level of glycated hemoglobin [HbA1c] >9.0%.
  • •Hypersensitivity to the studied product or any of its components, including lactose intolerance.
  • •The intake of any pharmaceutical agents with known influence on esophageal motility (including, but not limited to: beta-blockers, calcium channel blockers, m-cholinoblockers, myorelaxants, antidepressants, tranquilizers, prokinetic agents)
  • •Any medical conditions that may significantly affect life expectancy, including known cancers;
  • •Any clinically significant immunological, endocrine, hematological, gastrointestinal, neurological, tumor or psychiatric diseases;
  • •Mental instability or incapacity, which may impact the ability to give informed consent, take part in the study, or affect the ability to comply with the requirements of the study protocol;
  • •Inability to tolerate high-resolution esophageal manometry without sedation, at least in part.

Arms & Interventions

Arm 1

Experimental

Subjects of this arm will receive the following sequence of products: 1 - ice cream with brazzein, maltitol and oligofructose, 2 - ice cream with brazzein, erythritol, maltitol and inulin; 3 - standard ice cream

Intervention: specialized food based on ice cream, order 1 (Other)

Arm 2

Experimental

Subjects of this arm will receive the following sequence of products: 1 - ice cream with brazzein, erythritol, maltitol and inulin; 2 - ice cream with brazzein, maltitol and oligofructose, 3 - standard ice cream

Intervention: specialized food based on ice cream, order 2 (Other)

Arm 3

Experimental

Subjects of this arm will receive the following sequence of products: 1 - standard ice cream; 2 - ice cream with brazzein, maltitol and oligofructose, 3 - ice cream with brazzein, erythritol, maltitol and inulin

Intervention: specialized food based on ice cream, order 3 (Other)

Outcomes

Primary Outcomes

Mean contractile front velocity

Time Frame: baseline, during the intervention

CFV

Mean intrabolus pressure

Time Frame: baseline, during the intervention

IBP

Mean lower esophageal sphincter resting pressure

Time Frame: baseline, during the intervention

Based on the high-resolution esophageal manometry measurement

Distal contractile integral

Time Frame: baseline, during the intervention

mean lower esophageal sphincter integral relaxation pressure

Time Frame: baseline, during the intervention

IRP 4

Distal latency

Time Frame: baseline, during the intervention

DL

Secondary Outcomes

  • mean upper esophageal sphincter resting pressure(baseline, during the intervention)
  • product organoleptic assessment(during the intervention)
  • Mean upper esophageal sphincter integrated relaxation pressure(baseline, during the intervention)

Investigators

Sponsor
Federal State Budgetary Scientific Institution "Federal Research Centre of Nutrition, Biotechnology
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Sergey Morozov

Principal Investigator

Federal State Budgetary Scientific Institution "Federal Research Centre of Nutrition, Biotechnology

Study Sites (1)

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