Actively Recruiting
Fertility Preservation for Transfeminine Adolescents Via Semen Cryopreservation or Testicular Sperm Extraction
Led by Amsterdam UMC, location VUmc · Updated on 2024-05-06
40
Participants Needed
2
Research Sites
104 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The goal of this observational cohort study is to identify and predict parameters for successful testicular sperm extraction (TESE) procedures or semen cryopreservation more accurately and to evaluate the decision making process and the experience of postponing or temporarily discontinuing puberty suppression to undergo successful fertility preservation. in transfeminine (assigned male at birth) adolescents. The main question\[s\] it aims to answer are: * What is the optimal timing for fertility preservation before the start or after temporarily discontinuing puberty suppression puberty suppression * How do transfeminine adolescents and their parents experience the decision making process of fertility preservation * how do transfeminine adolescents and their parents experienced postponing or temporarily discontinuing puberty suppression to undergo successful fertility preservation? Participants will be asked to use their medical data, answer a questionnaire or participate in a (online) interview.
CONDITIONS
Official Title
Fertility Preservation for Transfeminine Adolescents Via Semen Cryopreservation or Testicular Sperm Extraction
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Before start of puberty suppresion with a wish for fertility preservation
- After discontinuing puberty suppersion before the start of hormone therapy
You will not qualify if you...
- Tanner stage > 4/5
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 2 locations
1
Amsterdam UMC, location AMC
Amsterdam, Netherlands, 1105 AZ
Actively Recruiting
2
Amsterdam UMC, Location VU Medical Center
Amsterdam, Netherlands
Actively Recruiting
Research Team
T
Tessa Stolk, MD
CONTACT
N
Norah van Mello, MD, PHD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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