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NCT06712485Not yet recruiting

Biomarkers in EV Associated With Marrow Adiposity in Anorexia

Identification of Biomarkers in Extracellular Vesicles Associated With Marrow Adiposity and Bone Deterioration Caused by Nutritional Deficiencies

Source: ClinicalTrials.gov · Last updated 7 May 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

The aim of this observational study is to identify biomarkers in extracellular vesicles associated with medullary adiposity occurring in patients with anorexia nervosa. The main question it aims to answer is: Can this medullary adiposity be associated with the bone deterioration observed in this population? Participants will be assessed for body composition and a blood sample will be taken by non-invasive techniques.

Status (registry)
Not yet recruiting
Study type
Observational
Enrollment
30 (estimated)
First submitted
26 Nov 2024
Start date
May 2025
Primary completion date
Dec 2025
Lead sponsor
Maimónides Biomedical Research Institute of Córdoba
NCT number
NCT06712485

What you commit to

  • Study type: Observational
  • Planned participants: 30
  • From May 2025 to the primary completion date, Dec 2025
  • 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.

Prior treatment

  • Not receiving oestrogens, contraceptives or glucocorticoids in the 3 months prior to the start of the study.

Other illness

  • Not to suffer from chronic diseases, such as diabetes, pathologies affecting the bone system or thyroid function.

Lab values

  • Do not take calcium or vitamin supplements.

Who the study is looking for

  • For AN group:
  • Diagnosis of active AN according to DSM-5 criteria
  • BMI of less than 17kg/m2
  • Present amenorrhoea in the 3 months prior to the start of the study.
    • For AN-R group:
  • Achieved weight gain of more than 85%.
  • Normal menstruation in the last 3 months.
    • For Control group:
  • Population of the same age and gender as the AN and AN-R groups.
  • If pubertal population, presenting a chronological age of ± 2 years.
  • Normal menstruation
  • Normal BMI (\>18.5 kg/m2)
  • No presence of previous dietary transtrons.

Sex: All · 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
Hospital Universitario Reina Sofía, Edificio IMIBIC, Avd. Menedez Pdial, s/n
Coordinator of this site? Confirm its status
CórdobaSpainUnknown status

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