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NCT07917364Recruiting

Asprosin and miRNA Expression in Young Women With Metabolic Syndrome

Association Between Serum Asprosin Concentration and Expression of Selected miRNAs With Risk Factors and Components of Metabolic Syndrome in Young Women: Diagnostic Perspectives

Source: ClinicalTrials.gov · Last updated 4 Nov 2026

Brief summary (registry, in English)

Metabolic syndrome is a major risk factor for cardiovascular disease and type 2 diabetes, and its prevalence in young adults is increasing. Early identification of individuals at risk may improve prevention strategies. This observational, cross-sectional case-control study investigates the relationship between serum asprosin concentration, the expression of six selected circulating microRNAs, and the components and risk factors of metabolic syndrome in young women aged 18 to 35 years. Two equally sized groups will be compared: women meeting NCEP ATP III criteria for metabolic syndrome and healthy age-matched controls. Participants attend a single study visit during which fasting blood samples, anthropometric and body composition measurements, blood pressure, and validated questionnaires assessing physical activity, diet, sleep quality, perceived stress, and quality of life are collected. The study aims to determine whether asprosin and the selected microRNA profile have diagnostic value as biomarkers of metabolic syndrome in this population.

Status (registry)
Recruiting
Study type
Observational
Enrollment
110 (estimated)
First submitted
16 Oct 2026
Start date
Nov 2026
Primary completion date
Mar 2027
Lead sponsor
University of Applied Sciences in Nowy Targ
Diseases
Obesity
NCT number
NCT07917364

What you commit to

  • Study type: Observational
  • Planned participants: 110
  • From Nov 2026 to the primary completion date, Mar 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Continuous pharmacotherapy for indications other than diabetes and/or hypertension, including any form of hormonal contraception (oral, transdermal, vaginal, implant, injectable or intrauterine)

Age

  • Age outside the range of 18 to 35 years

Other

  • Irregular menstrual cycle
  • Pregnancy or breastfeeding
  • Competitive sports training in any discipline
  • Current smoking
  • Alcohol abuse
  • Lack of written informed consent for study participation and processing of personal data

Who the study is looking for

  • Female sex
  • Age 18 to 35 years
  • Regular menstrual cycle
  • Not engaged in competitive sports training in any discipline
  • Non-smoker
  • No alcohol abuse
  • No continuous pharmacotherapy, with the exception of treatment for diabetes and/or antihypertensive treatment; no use of hormonal contraception
  • Written informed consent for study participation and processing of personal data

Age in the registry: 18 years to 35 years · Sex: Female · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Institute of Medicine, University of Applied Sciences in Nowy Targ, Kokoszków 71, 34-400 Nowy Targ, Poland
Coordinator of this site? Confirm its status
Nowy TargPolandRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.