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NCT Number: NCT06043609

Outcome Evaluation After Fertility Preservation

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.

Recruiting

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Key information

Age range

Up to 60 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Prince of Wales Hospital

Hong Kong

Location status: Recruiting

Location contact

Jacqueline Pui Wah CHUNG, MBBS

CONTACT

[email protected]

30501537

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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)

Treatment and study plan

This is an observational cohort study

Other

This is an observational cohort study

Primary outcomes

  1. To determine any factors that may affect the success rate of different fertility preservation methods.

    Time frame: 10 years

    The 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 outcomes

  1. To assess the pregnancy rate after different fertility preservation methods.

    Time frame: 10 years

    The medical notes of these patients undergoing fertility preservation services will be reviewed. The subsequent reproductive outcome will be obtained by reviewing their hospital record.

  2. To report on the frequency of surgical complications

    Time frame: 10 years

    The 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.

Study contacts

Contact information is provided by the study sponsor or research team.

Jacqueline CHUNG, MBBS

CONTACT

[email protected]

35051537

Sponsors and collaborators

Lead sponsor

Chinese University of Hong Kong

Other

Registry information

Important dates

Study start
2023
Primary completion
2033
Study completion
2035
First posted
Sep 21, 2023
Registry last updated
Jan 8, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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