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Study identifier: NCT06723938 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Phenotypic and Genotypic Characterisation of a Large, Multicentre Italian Cohort of 46, XY DSD Patients

Condition: 46, XY DSD  ·  Sponsor: IRCCS Azienda Ospedaliero-Universitaria di Bologna

PhaseN/A
Planned participants520
Who can joinAll sexes, N/A to 18 Years
Healthy volunteersNo

About this study

Observational exploratory study of a cohort of pediatric and adolescent patients diagnosed with DSD karyotype 46,XY, a rare congenital clinical condition characterized by a disharmonic development between chromosomal sex, gonadal sex and/or phenotypic sex.

This description comes directly from the study's public registry record.

Talk to the study team

Federico Baronio  ·  00390512144816  ·  federico.baronio@aosp.bo.it

Always discuss trial participation with your own doctor first.

Locations (4)

IRCCS Azienda Ospedaliero-Universitaria di BolognaBologna, Bologna, ItalyRecruiting
IRCCS Ospedale San RaffaeleMilan, Milano, ItalyNot Yet Recruiting
Azienda Ospedaliero Universitaria PisanaPisa, Pisa, ItalyNot Yet Recruiting
Ospedale Pediatrico Bambino GesùRoma, Roma, ItalyNot Yet Recruiting

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Source record: clinicaltrials.gov/study/NCT06723938