RecruitingPhase 4NCT06544473
Determining Dose Equivalence Between Oral and Transdermal Estrogen Treatment in Women With Turner Syndrome
Studying Turner syndrome
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Aarhus University Hospital
- Principal Investigator
- Claus H Gravholt, ProfessorAarhus University Hospital
- Intervention
- 17-beta estradiol(drug)
- Enrollment
- 50 enrolled
- Eligibility
- 18-50 years · FEMALE
- Timeline
- 2021 – 2026
Study locations (1)
- Department of Endocrinology and Internal Medicine, Aarhus University Hospital, Aarhus, Aarhus N, Denmark
Collaborators
University of Aarhus
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.
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