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NCT05237440Recruiting

Childhood Traumas in Obese Women: Association With Deregulation of the Glucocorticoid Axis and Inflammatory State.

Source: ClinicalTrials.gov · Last updated 26 Jun 2026

Brief summary (registry, in English)

We postulate that childhood traumas are associated with deregulation of the glucocorticoid axis and the inflammatory system in obese women. The main objective of the study is to compare the salivary cortisol awaking response in obese women according to the presence of childhood trauma (assessed using the Childhood Trauma Questionnaire, CTQ).

Status (registry)
Recruiting
Study type
Interventional
Enrollment
102 (estimated)
First submitted
7 Jan 2022
Start date
13 Apr 2022
Primary completion date
13 May 2027
Lead sponsor
University Hospital, Limoges
Diseases
Obesity
NCT number
NCT05237440

What you commit to

  • Study type: Interventional
  • Planned participants: 102
  • From 13 Apr 2022 to the primary completion date, 13 May 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.

Prior treatment

  • Subjects with a positive diagnosis of hypercorticism or suspected hypercorticism will also be excluded: 8-hour plasma cortisol after Dexamethasone suppression test (DST) (1 mg dexamethasone taken orally at midnight the previous day) greater than 1.8 microg/100 ml (50 nmol/l)
  • treatment(s) likely to modify the exploration of the corticotropic axis: systemic or local corticosteroid therapy or glucocorticoid infiltration for less than 6 months
  • current use of anti-inflammatory drugs or antibiotics

Other illness

  • History of bariatric surgery
  • Any condition or pathology that may influence the corticotropic axis or that may modify the excretion or dosage of cortisol:
    • pregnancy, breastfeeding
    • hepatocellular insufficiency,
    • severe heart failure,
    • mild/moderate acute heart failure,
    • any psychological disorder not stabilised for at least one year
    • alcohol or drug dependence, not weaned for at least one year
    • neoplasm under treatment
  • Current infectious disease or a history of autoimmune disease (except autoimmune hypothyroidism), inflammatory disease and/or neurodegenerative disease
  • Presence of an adrenal adenoma or any known or suspected clinical adrenal or corticotropic disorder

Other

  • antidepressant and neuroleptic treatment, benzodiazepine treatment
  • Shift worker

Who the study is looking for

  • ≥18 years female BMI≥30kg/m2

Age in the registry: 18 years to - · Sex: Female · Does not accept 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
LimogesUniversity Hospital
Coordinator of this site? Confirm its status
LimogesFranceRecruiting

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