Stopped: replaced by other study
Prospective observational study and biobank in all persons referred to CKIO * Patient involvement and quality of life * Population characteristics regarding hormone levels, safety parameters and clinical outcome before and after gender affirming hormone treatment.
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Patient reported outcomes (PRO)
Timeframe: Every 52 weeks
Hormone levels
Timeframe: Every 52 weeks
Safety parameters
Timeframe: Every 52 weeks