Actively Recruiting
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
Eligibility Criteria
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
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
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
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
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
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