Inulin in Burn-induced Insulin Resistance
Primary Purpose
Burn Injury, Insulin Resistance, Post Burn Insulin Resistance
Status
Not yet recruiting
Phase
Not Applicable
Locations
Serbia
Study Type
Interventional
Intervention
Inulin 20 mg
Placebo
Sponsored by
About this trial
This is an interventional treatment trial for Burn Injury
Eligibility Criteria
Inclusion Criteria:
- Informed consent and willingness in study participation
- The age of the respondent greater than or equal to 18 years at the time of signing the informed consent
- Burns requiring in-hospital treatment
- insulin resistance detected on the fifth day of admission to the hospital
Exclusion Criteria:
- Documented pre-existing insulin resistance
- PCOS
- BMI ≥ 30 kg/m2
- Pregnancy
- Diabetes type 1
- Diabetes type 2
- Metabolic syndrome
- Use of drugs that can affect insulin resistance
- Weight loss greater than 10% in the last 6 months
Sites / Locations
- Faculty of Medicine; Clinical Center of Serbia, Clinic for Burns, Plastic and Reconstructive Surgery
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
Inulin 20 mg
Placebo
Arm Description
Inulin 20 mg administrated orally q24h
Matching placebo q24h
Outcomes
Primary Outcome Measures
Changes in insulin resistance measured by HOMA-IR
Changes in insulin resistance in placebo and experimental group measured by HOMA-IR
Change in fasting plasma glucose level
Changes in fasting plasma glucose in placebo and experimental group
Change in plasma insulin level
Change in plasma insulin levelin placebo and experimental group
Changes in insulin resistance measured by QUICKI
Changes in insulin resistance in placebo and experimental group measured by QUICKI
Changes in HbA1c level
Changes in HbA1c level in placebo and experimental group
Secondary Outcome Measures
Survival
The survival of patient in placebo and experimental group
Burn wound changes
The change in diameter, tissue type and contraction of wound in placebo and experimental group
Development of local and systemic infection
The developement of local and systhemic infection in placebo and experimental group
Full Information
NCT ID
NCT05532488
First Posted
September 4, 2022
Last Updated
September 4, 2022
Sponsor
University of Belgrade
1. Study Identification
Unique Protocol Identification Number
NCT05532488
Brief Title
Inulin in Burn-induced Insulin Resistance
Official Title
The Inulin Effect on Burn-induced Insulin Resistance: a Randomized, Double-blind Placebo-controlled Pilot Trial
Study Type
Interventional
2. Study Status
Record Verification Date
September 2022
Overall Recruitment Status
Not yet recruiting
Study Start Date
August 1, 2023 (Anticipated)
Primary Completion Date
January 31, 2024 (Anticipated)
Study Completion Date
January 31, 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Belgrade
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
5. Study Description
Brief Summary
In this clinical trial, investigators will test the effects of dietary supplement inulin, on the reduction of insulin resistance developed as a result of burn injuryy.
Detailed Description
As a consequence of burn injury, an exaggerated inflammatory response is developing in parallel with metabolic changes, which led to the development of hyperglycemia and insulin resistance. The post burn-injury insulin resistance is different in comparison to other trauma-induced insulin resistance. The main difference is the length. More precisely postburn-injury insulin resistance lasts longer than insulin resistance developed after other traumas. Insulin resistance can persist for years after the burn heals.
Inulin is a heterogeneous mixture of fructose polymers that are widely distributed in nature as storage of carbohydrates in plants. This mixture of fructose has nutritional value, but also affects general health, reducing the risk of developing various diseases. Inulin prevents gastrointestinal complications such as constipation, increases the resorption of minerals from the gastrointestinal tract, stimulates the immune system, and functions as a prebiotic, but can also affect insulin resistance in patients with metabolic syndrome.
The hypothesis: The everyday inulin can affect postburn-injury insulin resistance.
To investigate the effect of inulin on patients with postburn-injury insulin resistance a prospective, double-blind, randomized, and placebo-controlled clinical trial will be performed. This initial trial is a pilot trial. The pilot trial will be performed to assess the safety of treatment or interventions and recruitment potentials, examine the randomization and blinding process, increase the researchers' experience with the study methods and interventions, and provide estimates for sample size calculation for the main study.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Burn Injury, Insulin Resistance, Post Burn Insulin Resistance
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
40 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Inulin 20 mg
Arm Type
Experimental
Arm Description
Inulin 20 mg administrated orally q24h
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Matching placebo q24h
Intervention Type
Dietary Supplement
Intervention Name(s)
Inulin 20 mg
Intervention Description
Inulin can increase gut Bifidobacterium count. Bifidobacterium has beneficial effects on the metabolic profile and insulin resistance biomarkers.
Intervention Type
Other
Intervention Name(s)
Placebo
Intervention Description
Placebo
Primary Outcome Measure Information:
Title
Changes in insulin resistance measured by HOMA-IR
Description
Changes in insulin resistance in placebo and experimental group measured by HOMA-IR
Time Frame
Baseline and end of the study (6week)
Title
Change in fasting plasma glucose level
Description
Changes in fasting plasma glucose in placebo and experimental group
Time Frame
Baseline and end of the study (6week)
Title
Change in plasma insulin level
Description
Change in plasma insulin levelin placebo and experimental group
Time Frame
Baseline and end of the study (6week)
Title
Changes in insulin resistance measured by QUICKI
Description
Changes in insulin resistance in placebo and experimental group measured by QUICKI
Time Frame
Baseline and end of the study (6week)
Title
Changes in HbA1c level
Description
Changes in HbA1c level in placebo and experimental group
Time Frame
Baseline and end of the study (6week)
Secondary Outcome Measure Information:
Title
Survival
Description
The survival of patient in placebo and experimental group
Time Frame
6 weeks
Title
Burn wound changes
Description
The change in diameter, tissue type and contraction of wound in placebo and experimental group
Time Frame
6 weeks
Title
Development of local and systemic infection
Description
The developement of local and systhemic infection in placebo and experimental group
Time Frame
6 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Informed consent and willingness in study participation
The age of the respondent greater than or equal to 18 years at the time of signing the informed consent
Burns requiring in-hospital treatment
insulin resistance detected on the fifth day of admission to the hospital
Exclusion Criteria:
Documented pre-existing insulin resistance
PCOS
BMI ≥ 30 kg/m2
Pregnancy
Diabetes type 1
Diabetes type 2
Metabolic syndrome
Use of drugs that can affect insulin resistance
Weight loss greater than 10% in the last 6 months
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Marko A Stojanović, MD, PhD
Phone
00381601435353
Email
stojanovic.dr.marko@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Marko A Stojanović, MD, PhD
Organizational Affiliation
Faculty of Medicine, University of Belgrade
Official's Role
Principal Investigator
Facility Information:
Facility Name
Faculty of Medicine; Clinical Center of Serbia, Clinic for Burns, Plastic and Reconstructive Surgery
City
Belgrade
ZIP/Postal Code
11000
Country
Serbia
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Marko A Stojanović, MD, PhD
Phone
00381601435353
Email
marko.stojanovic@med.bg.ac.rs
12. IPD Sharing Statement
Plan to Share IPD
Yes
IPD Sharing Plan Description
The study protocol will be published before the beginning of the study. All of the other necessary information regarding the study will be available at Zenodo repository before publishing the data.
IPD Sharing Time Frame
The date of interest will be available at the beginning of study and at least three years after the termination of the study
IPD Sharing Access Criteria
On demanded
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Inulin in Burn-induced Insulin Resistance
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