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The Effects of Butyrate on Children With Obesity

Primary Purpose

Insulin Resistance, Obesity

Status
Unknown status
Phase
Phase 2
Locations
Italy
Study Type
Interventional
Intervention
Butyrate
Placebo
Sponsored by
Federico II University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Insulin Resistance

Eligibility Criteria

7 Years - 15 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Obesity (BMI >95° percentile)
  • HOmeostasis Model Assessment (HOMA-IR) > 4 (obtained by calculating the product of fasting plasma insulin expressed in microunits/mL and fasting plasma glucose expressed in mmol/L divided by 22.5)

Exclusion Criteria:

  • Age <10 or >15 years
  • BMI <95° centile
  • HOMA-IR <4
  • Patients under pharmacological treatment for obesity (metformin) or taking vitamin E, pre-, pro- or synbiotics
  • Simultaneous presence of other chronic diseases unrelated to obesity (cancer, immunodeficiency, cystic fibrosis, allergies, celiac disease, autoimmune diseases, neuropsychiatric disorders, type 1 diabetes, inflammatory bowel diseases, malformations of urinary or gastrointestinal or respiratory tract, chronic lung diseases, genetic and metabolic diseases, chronic hematological diseases)
  • History of surgery for the treatment of obesity
  • Any medical condition that may interfere with participation in this study
  • Participation in other clinical trials still in progress

Sites / Locations

  • University of Naples Federico IIRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Hypocaloric diet plus butyrate

Hypocaloric diet plus placebo

Arm Description

Hypocaloric diet plus butyrate

Hypocaloric diet plus placebo

Outcomes

Primary Outcome Measures

Reduction of insulin resistance

Secondary Outcome Measures

Reduction of body weight

Full Information

First Posted
March 23, 2016
Last Updated
March 29, 2016
Sponsor
Federico II University
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1. Study Identification

Unique Protocol Identification Number
NCT02721953
Brief Title
The Effects of Butyrate on Children With Obesity
Official Title
Effects of Butyrate on Insulin Resistance in Children Affected by Obesity
Study Type
Interventional

2. Study Status

Record Verification Date
March 2016
Overall Recruitment Status
Unknown status
Study Start Date
March 2016 (undefined)
Primary Completion Date
January 2018 (Anticipated)
Study Completion Date
March 2018 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Federico II University

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Butyrate is a short chain fatty acid (SCFA) produced by bacterial fermentation of undigested starch in the gut. Butyrate carries out different effects at intestinal and extraintestinal level, including: immune regulation with anti-inflammatory effect at intestinal and systemic level and modulation of gut microbiota. Many of these effects result from an epigenetic mechanism. Shown in an animal model of obesity induced by a high fat diet (HFD), that butyrate can exercise very effective protective action against obesity through the stimulation of intestinal satiety hormones. Shown always in murine model of obesity induced by HFD, that butyrate is effective in preventing and treating obesity and insulin resistance. After 5 weeks of treatment with butyrate was observed a reduction of 10.2% of body weight, 30% of fasting glucose and 50% insulin resistance. In an animal model of metabolic syndrome with NAFLD researchers have recently demonstrated that the administration of butyrate is able to significantly reduce insulin resistance, liver damage, dyslipidaemia through a modulation of the inflammatory process. Pharmacokinetic and pharmacodynamic studies in humans show that the oral administration of butyrate is safe and well tolerated. The peak serum levels occurs 4-6 hours after oral administration. All of these data makes plausible a possible positive effect on insulin resistance in the obese child.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Insulin Resistance, Obesity

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
40 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Hypocaloric diet plus butyrate
Arm Type
Experimental
Arm Description
Hypocaloric diet plus butyrate
Arm Title
Hypocaloric diet plus placebo
Arm Type
Placebo Comparator
Arm Description
Hypocaloric diet plus placebo
Intervention Type
Dietary Supplement
Intervention Name(s)
Butyrate
Intervention Description
Butyrate
Intervention Type
Other
Intervention Name(s)
Placebo
Intervention Description
Placebo
Primary Outcome Measure Information:
Title
Reduction of insulin resistance
Time Frame
After 6 months of treatment
Secondary Outcome Measure Information:
Title
Reduction of body weight
Time Frame
After 6 months of treatment

10. Eligibility

Sex
All
Minimum Age & Unit of Time
7 Years
Maximum Age & Unit of Time
15 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Obesity (BMI >95° percentile) HOmeostasis Model Assessment (HOMA-IR) > 4 (obtained by calculating the product of fasting plasma insulin expressed in microunits/mL and fasting plasma glucose expressed in mmol/L divided by 22.5) Exclusion Criteria: Age <10 or >15 years BMI <95° centile HOMA-IR <4 Patients under pharmacological treatment for obesity (metformin) or taking vitamin E, pre-, pro- or synbiotics Simultaneous presence of other chronic diseases unrelated to obesity (cancer, immunodeficiency, cystic fibrosis, allergies, celiac disease, autoimmune diseases, neuropsychiatric disorders, type 1 diabetes, inflammatory bowel diseases, malformations of urinary or gastrointestinal or respiratory tract, chronic lung diseases, genetic and metabolic diseases, chronic hematological diseases) History of surgery for the treatment of obesity Any medical condition that may interfere with participation in this study Participation in other clinical trials still in progress
Facility Information:
Facility Name
University of Naples Federico II
City
Naples
ZIP/Postal Code
80131
Country
Italy
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Roberto Berni Canani, MD, PhD
Phone
+390817462680

12. IPD Sharing Statement

Plan to Share IPD
No

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The Effects of Butyrate on Children With Obesity

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