Actively Recruiting
Outcome Evaluation After Fertility Preservation
Led by Chinese University of Hong Kong · Updated on 2026-01-08
100
Participants Needed
1
Research Sites
104 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are evaluating the outcomes of different fertility preservation strategies in patients who have undergone or will seek such services. The study aims to identify factors that may influence the success of these fertility preservation methods, focusing on patients with conditions or treatments that could harm their fertility. This research is observational and involves reviewing medical records without requiring extra procedures from participants. Participants include patients seeking fertility preservation consultation or those returning to use their frozen gametes or embryos. The study collects baseline information like socio-demographic background, medical history, surgical details, and reproductive outcomes by reviewing hospital records. There are no interventions or treatments assigned, as this is a cohort observational study. Participants are involved through medical record assessments during their routine consultations or follow-ups at the hospital. Researchers track outcomes such as pregnancy rates, surgical complications, and factors affecting the success of fertility preservation methods over a 10-year period. The study does not require additional visits or procedures beyond standard care.
CONDITIONS
Brief Title
Outcome Evaluation After Fertility Preservation
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients aged from 0-50 years old
- Patients with any illness or treatment that may cause irreversible fertility damage, including extensive abdominal surgery or high toxicity medication
- Patients seeking fertility preservation services
You will not qualify if you...
- Patients unable to provide consent or assent due to significant psychiatric problems or cognitive delay
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person) at fertility preservation consultation
Duration - Up to 10 years
Participants who have undergone fertility preservation services are observed through medical record assessments to evaluate reproductive outcomes and surgical complications over time.
No additional visits; assessments are based on medical record reviews
Trial Site Locations
Total: 1 location
1
Prince of Wales Hospital
Hong Kong, Hong Kong
Actively Recruiting
Research Team
J
Jacqueline CHUNG, MBBS
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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