Evaluating outcomes after fertility preservation methods
Outcome Evaluation After Fertility Preservation
Chinese University of Hong Kong · NCT06043609
This study looks at how well different fertility preservation methods work for people who have had cancer or other fertility issues, using their medical records to see what factors might affect their success.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 100 (estimated) |
| Ages | N/A to 60 Years |
| Sex | All |
| Sponsor | Chinese University of Hong Kong (other) |
| Locations | 1 site (Hong Kong) |
| Trial ID | NCT06043609 on ClinicalTrials.gov |
What this trial studies
This observational study aims to assess the reproductive outcomes of patients who have undergone various fertility preservation strategies due to cancer or other fertility issues. Participants will be invited from the Prince of Wales Hospital, where their medical records will be reviewed to gather baseline characteristics and subsequent reproductive outcomes. The study focuses on understanding how different factors may influence the success of fertility preservation efforts without requiring additional procedures from participants.
Who should consider this trial
Good fit: Ideal candidates for this study are patients aged 0-50 who are seeking fertility preservation services due to conditions that may harm their fertility.
Not a fit: Patients who are unable to provide consent due to significant psychiatric problems or cognitive delays may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could provide valuable insights into the effectiveness of fertility preservation methods, helping patients make informed decisions about their reproductive health.
How similar studies have performed: Other studies have shown success in evaluating fertility preservation outcomes, making this approach both relevant and valuable.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patients aged from 0-50 years old * Patients with any illness or who will undergo any type of treatment that may cause irreversible damage to their fertility, such as extensive abdominal surgery, high toxicity medication and treatments; * Patients seek for fertility preservation services Exclusion Criteria: -Patients unable to provide consent/assent (i.e. significant psychiatric problems/cognitive delay)
Where this trial is running
Hong Kong
- Prince of Wales Hospital — Hong Kong, Hong Kong (RECRUITING)
Study contacts
- Principal investigator: Jacqueline CHUNG, MBBS — Chinese University of Hong Kong
- Study coordinator: Jacqueline CHUNG, MBBS
- Email: jacquelinechung@cuhk.edu.hk
- Phone: 35051537
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Cancer, Fertility Issues