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RecruitingNCT06794190

Characterization of Hepatopathy in Turner Syndrome: Analysis of Determinants

Characterization of Hepatopathy in Turner Syndrome: Analysis of Determinants in an Observational Study

Status
Recruiting
Phase
Study type
Observational
Enrollment
120 (estimated)
Sponsor
IRCCS Azienda Ospedaliero-Universitaria di Bologna · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Not accepted

Summary

The present study is therefore aimed at investigating the prevalence of hepatic alterations (laboratory and imaging) in adult patients with TS and generating hypothesissto the possible etiopathogenetic factors most involved, as well as evaluating the correlation between biochemical and structural abnormalities. Thus, the study could provide relevant etiopathogenetic and prognostic results on the development of hepatopathy in TS patients.

Detailed description

The study is an observational retrospective cohort type; patients with TS in longitudinal monitoring at the U.O.C. of Endocrinology and Diabetes Prevention and Care, DIMEC, of IRCCS Policlinico S. Orsola of Bologna will be enrolled. The diagnosis of TS was made for most patients by the Pediatrics unit of Policlinico S. Orsola; in rare cases it was performed in adulthood by our operating unit or at another center; in all cases, the diagnosis was made by karyotype analysis on peripheral blood. The patients, as per clinical practice, underwent clinical evaluation with measurement of anthropometric parameters; an evaluation of the patients' medical history will be performed, paying attention to possible diagnosis of metabolic comorbidities and autoimmune diseases. Complete information regarding the history of menstrual cycles and replacement therapies used will also be collected. Finally, laboratory investigations are planned.

Conditions

Timeline

Start date
2025-01-07
Primary completion
2026-01-06
Completion
2026-01-07
First posted
2025-01-27
Last updated
2025-01-27

Locations

1 site across 1 country: Italy

Source: ClinicalTrials.gov record NCT06794190. Inclusion in this directory is not an endorsement.