Outcome Evaluation After Fertility Preservation
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
AgeUp to 60
SponsorChinese University of Hong Kong
About this trial
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.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
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
Disqualifiers
None
Trial population
All patients who have undergone or will seek for fertility preservation services in PWH will be invited to participate.
Trial design
Design model
Case-only
Time perspective
Prospective
Treatments tested in this trial
This is an observational cohort study
Other interventionThis is an observational cohort study
Treatment groups
No treatment groups listed
Trial outcomes
Primary outcomes
1
To determine any factors that may affect the success rate of different fertility preservation methods.
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.
Time frame
10 yearsSecondary outcomes
1
To assess the pregnancy rate after different fertility preservation methods.
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.
Time frame
10 years2
To report on the frequency of surgical complications
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.
Time frame
10 yearsSponsors and contacts
Click on the lead sponsor to view all of their trials.
Source ClinicalTrials.gov