Skip to content

Outcome Evaluation After Fertility Preservation

Outcome Evaluation After Fertility Preservation

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06043609
Enrollment
100
Registered
2023-09-21
Start date
2023-09-21
Completion date
2035-10-01
Last updated
2026-01-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cancer, Fertility Issues

Brief summary

It is important to evaluate outcomes after different fertility preservation strategies. Therefore, this study aims to assess the outcomes after different fertility preservation strategies and identify any factors that may affect their reproductive outcome.

Detailed description

All patients who have undergone or will seek fertility preservation services in PWH will be invited to participate. For those patients who have undergone fertility preservation services in PWH, when they come back to use their frozen gametes or embryos, they will also be invited to participate. Medical record assessment When patients come for fertility preservation consultation in PWH, they will be invited to participate. The medical notes of these patients undergoing fertility preservation services will be reviewed. The baseline characteristics including the socio-demographic background, past medical history, details of the surgical procedures, and the subsequent reproductive outcome, will be obtained by reviewing their hospital record. The participants will not be required to take any extra procedures.

Interventions

OTHERThis is an observational cohort study

This is an observational cohort study

Sponsors

Chinese University of Hong Kong
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
No minimum to 60 Years
Healthy volunteers
No

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)

Design outcomes

Primary

MeasureTime frameDescription
To determine any factors that may affect the success rate of different fertility preservation methods.10 yearsThe medical notes of these patients undergoing fertility preservation services will be reviewed. The baseline characteristics including the socio-demographic background will be obtained by reviewing their hospital record.

Secondary

MeasureTime frameDescription
To assess the pregnancy rate after different fertility preservation methods.10 yearsThe medical notes of these patients undergoing fertility preservation services will be reviewed. The subsequent reproductive outcome will be obtained by reviewing their hospital record.
To report on the frequency of surgical complications10 yearsThe medical notes of these patients undergoing fertility preservation services will be reviewed. The details of the surgical procedures will be obtained by reviewing their hospital record.

Countries

Hong Kong

Contacts

Primary ContactJacqueline CHUNG, MBBS
jacquelinechung@cuhk.edu.hk35051537

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026