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Clinical Trials/NCT07083427
NCT07083427Not yet recruitingNot Applicable

CAPA In-vitro Oocyte Maturation

Chinese University of Hong Kong1 site in 1 country50 target enrollmentStarted: August 1, 2025Last updated:

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Enrollment
50
Locations
1
Primary Endpoint
Number of mature oocytes

Study Overview

Brief Summary

In vitro oocyte maturation (IVM) is a mild-approach assisted reproductive technology (ART). Because of its simplicity, the more favorable financial implications (reduced cost) for patients, and the lower health risk profile of IVM compared to controlled ovarian stimulation (COS) in polycystic ovary syndrome (PCOS) patients, the use of IVM in selected patients may gain increasing interest. Besides its application in patients with polycystic ovaries, IVM technology may have a role in fertility preservation, where young girls and adult women are facing infertility due to gonadotoxic chemotherapeutic treatment.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Other
Masking
None

Eligibility Criteria

Ages
18 Years to 50 Years (Adult)
Sex
Female
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Patients aged from 18-50 years old
  • Patients seek fertility preservation services
  • Patients seek oocyte retrieval services

Exclusion Criteria

  • Patients unable to provide consent/assent (i.e. significant psychiatric problems/cognitive delay)

Outcomes

Primary Outcomes

Number of mature oocytes

Time Frame: 1 week

Number of mature oocytes after IVM

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Chung Pui Wah Jacqueline

Associate Professor

Chinese University of Hong Kong

Study Sites (1)

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