- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06152068
Insulin Resistance, Lipid Profile, CRP, IL-18 and Carotid Intima-Media Thickness (CIMT) Diameter in Obese Adolescents (CIMT)
Carotid intima-media thickness (CIMT) is a marker for detecting endothelium dysfunction, and has become a non-invasive method that is very useful in detecting and evaluating subclinical atherosclerosis in obese children and adolescents. This method is very useful in visually detecting and monitoring changes in the intima and its medial thickness, and can also evaluate changes within the arterial wall in the absence of localized plaque. Previous research that was conducted found an increase in CIMT diameter in 44 of 59 obese adolescents. Obesity has a risk of increasing the diameter of CIMT which carries the risk of atherosclerosis. Obesity accompanied by insulin resistance, and metabolic syndrome has a greater risk of atherosclerosis. Currently, the prevalence of obesity in adolescents is increasing. Interleukin 18 is a group of interleukin 1 whose levels increase in chronic inflammatory processes such as obesity, metabolic syndrome, and type 2 diabetes mellitus. IL-18 levels increase in obesity with increased CIMT.
Assessment of cardiovascular risk in obese adolescents is still a challenge for health practitioners, to prevent cardiovascular complications in obese adolescents which can cause sudden death at a young age. It is necessary to assess changes in the cardiovascular system that can be identified early by knowing the CIMT diameter. However, there is no definite reference value so the CIMT can be used as a reference for the occurrence of subclinical atherosclerosis in obese adolescents. In the previous study, CIMT was not examined in non-obese adolescents, so the cut-off for CIMT in non-obese was not known. Therefore, we have the opportunity to research to determine the thickness of CIMT and determine the cut-off value of CIMT which is at risk of experiencing early atherosclerosis in the obese adolescent population.
Study Overview
Status
Conditions
Detailed Description
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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East Java
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Surabaya, East Java, Indonesia, 61318
- RS Bhayangkara Surabaya
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Adolescents (obese and normal)
- Aged 13-18 years old
- Not Smoking
- Not consumed alcohol and drugs
Exclusion Criteria:
- Suffering from infections, inflammation, autoimmune diseases, cancer, chronic diseases, and endocrine disorders
- consuming steroids or hormone therapy
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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Obesity
Subjects with obesity were assessed with body mass index or BMI (calculated with body weight in kg divided by body height square in m).
The subjects were determined to be obese if BMI value z-score > +2 SD of WHO child growth standard (assessed with WHO Anthroplus).
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non-obesity
Subjects non-obesity were assessed with body mass index or BMI (calculated with body weight in kg divided by body height square in m).
The subjects were determined to be non-obesity if BMI value z-score < +2 SD of WHO child growth standard (assessed with WHO Anthroplus).
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Body Mass Index (BMI)
Time Frame: 5 months
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BMI was calculated by dividing body weight (in kg) by body height square (in m) [body weight (kg)/body height2 (m2)], in kg/m2 unit.
The data will be presented as mean +/- standard deviation (SD)
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5 months
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Fasting insulin
Time Frame: 5 months
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Blood samples were collected at 08.00-09.00
after the subject fasted for 12 hours through the median cubital vein.
Ten ml of blood was taken.
The blood sample collection was done by a laboratory's employers or a nurse who had been hired by the researchers.
After the blood was taken, it was placed into a tube containing ethylenediaminetetraacetic acid (EDTA) for further analysis of Fasting insulin (FI).
After that, the tube containing blood samples was placed in a cooling box for transport to the lab.
The data will be presented as mean +/- SD, in μU/mL.
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5 months
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Body weight
Time Frame: 5 months
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The data will be presented as mean +/- SD (standard deviation). The body weight will be measure with Seca electronic flat scale 813, in kg. (in grams) for subjects >24 months age. |
5 months
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Body height
Time Frame: 5 months
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The data will be presented as mean +/- SD (standard deviation).
The body height was measured using stadiometer Seca 213 (in cm).
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5 months
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Blood pressure
Time Frame: 5 months
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blood pressure was measure using Omron Automatic Blood Pressure Monitor (Omron Health Care Co., Ltd, Japan) (in mmHg), by placing the cuff on the right arm, then pull and tighten it according to the size if the arm.
After it was installed correctly (fasten and did not move), the power button on the digital tension tool was pressed, and then the microprocessor started to drive air pressure into the cuff, and then the value of blood pressures will appear in the manometer tube column.
Systolic blood pressure measurement was performed in a sitting position after the subject had rested for 10 minutes.
The data will be presented as mean +/- standard deviation (SD)
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5 months
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Carotid Intima Media Thickness
Time Frame: 5 months
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A CIMT test uses ultrasound technology to create images of your artery layers.
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5 months
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Nur Aisiyah Widjaja, Ph.D, Child Health Department, Faculty of Medicine, Universitas Airlangga
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Forth ID
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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