Actively Recruiting

Age: 18Years - 46Years
FEMALE
ID07546123

Ovarian Tissue Cryopreservation Combined With Oocyte Cryopreservation Versus Oocyte Cryopreservation Alone: an Observational Study in Oncology Patients

Led by IRCCS Azienda Ospedaliero-Universitaria di Bologna · Updated on 2026-04-22

127

Participants Needed

1

Research Sites

8 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This research aims to evaluate fertility preservation methods for female cancer patients who will undergo treatments that may harm their ovarian reserve, such as chemotherapy, radiotherapy, or surgery. The study compares two approaches: ovarian tissue cryopreservation combined with oocyte cryopreservation versus oocyte cryopreservation alone, to better understand how to protect fertility before gonadotoxic therapy. Participants will be divided into two groups based on their planned cancer treatment and available time before therapy starts. One group will undergo ovarian tissue freezing followed by egg freezing, while the other group will have only egg freezing. The study collects data from both retrospective and prospective participants over a period of more than four years. During the study, researchers will monitor the number of eggs retrieved, the rate of egg retrieval compared to follicles aspirated, mature egg counts, and the occurrence of moderate ovarian hyperstimulation syndrome after retrieval. Blood hormone levels will also be analyzed to see their relation to egg yield. Safety events such as infections or internal bleeding will be tracked. Participation involves monitoring before and after egg retrieval, with total enrollment lasting several years.

CONDITIONS

Brief Title

Ovarian Tissue Cryopreservation Combined With Oocyte Cryopreservation Versus Oocyte Cryopreservation Alone

Who Can Participate

Age: 18Years - 46Years
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Patient with oncological disease eligible for potentially gonadotoxic therapy
  • Body mass index (BMI) between 17.5 and 32 kg/m²
  • Age between 18 and 46 years
  • Female gender
Not Eligible

You will not qualify if you...

  • Allergy to any of the active substances used during ovarian stimulation treatment
  • Positive test for hepatitis B virus (HBV), hepatitis C virus (HCV), human immunodeficiency virus (HIV), or Treponema pallidum
  • Lack of clearance for oncological treatment from a doctor or specialist
  • Male gender or outside age range 18-46 years
  • Body mass index (BMI) outside 17.5 to 32 kg/m² range

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Monitoring

Duration - Up to 7 days after oocyte retrieval

Participants undergo observation to compare fertility preservation methods before gonadotoxic therapy.

1 visit at oocyte retrieval and 1 visit within 7 days after retrieval

Trial Site Locations

Total: 1 location

1

IRCCS Azienda Ospedaliero-Universitaria di Bologna

Bologna, Bologna, Italy, 40138

Actively Recruiting

Loading map...

Research Team

D

Diego Raimondo, MD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

Similar Trials

Antimüllerian Hormone as a Predictor of Future Infertility R...

Fertility Preservation

Actively Recruiting

10 locations

Frequently Asked Questions

Have more questions? Get in touch with our team for quick support

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here