RecruitingNCT06754423

Electronic Registry of Male Patients With Congenital Adrenal Hyperplasia 21-hydroxylase Deficiency

Studying Congenital adrenal hyperplasia

Last synced from ClinicalTrials.gov

Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing data

Key facts

Sponsor
IRCCS Azienda Ospedaliero-Universitaria di Bologna
Principal Investigator
Alessandra Gambineri, MD
IRCCS Azienda Ospedaliero-Universitaria di Bologna
Enrollment
30 enrolled
Eligibility
18 years · MALE
Timeline
20222032

Study locations (1)

Primary source

Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.

Open NCT06754423 on ClinicalTrials.gov

Other trials for Congenital adrenal hyperplasia

Additional recruiting or active studies for the same condition.

See all trials for Congenital adrenal hyperplasia

← Back to all trials