Actively Recruiting
Fertility Preservation in Young Women With Cancer: an International Registration Study From the International Network on Cancer, Infertility and Pregnancy (INCIP)
Led by University Hospital, Gasthuisberg · Updated on 2020-11-18
2000
Participants Needed
2
Research Sites
N/A
Total Duration
On this page
Sponsors
U
University Hospital, Gasthuisberg
Lead Sponsor
N
NKI-AvL
Collaborating Sponsor
AI-Summary
What this Trial Is About
This research focuses on young women with cancer who are receiving fertility preserving cancer treatments. The study aims to track how often these treatments are used, the types of treatments given, and the long-term outcomes related to both cancer and fertility. It compares results from women receiving fertility sparing treatments to those undergoing standard cancer treatments. The study is an international, multicenter prospective observational trial designed to improve understanding of the safety and effectiveness of fertility preservation in cancer care. Participants in this study are young women with cancer who choose fertility preserving treatments during their cancer care. These treatments may vary across centers and deviate from standard protocols to protect fertility while treating cancer. The study records detailed information about cancer diagnosis, treatment methods, and both oncological and fertility outcomes over time. All patients receive fertility sparing cancer treatment based on their specific request. During the study, researchers collect data on cancer diagnosis, treatment, and outcomes, focusing on both cancer control and fertility preservation. The primary outcome measured is fertility outcome over 10 years, while oncological outcomes are tracked over 5 years. Participants provide written consent, and the study follows them long term to understand the effects of fertility preserving cancer treatments on survival and reproductive health. The total participation duration spans multiple years for ongoing follow-up.
CONDITIONS
Brief Title
Fertility Preservation in Young Women With Cancer
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Young women who want to preserve their fertility during cancer treatment
- Patients must provide signed and written informed consent to participate
You will not qualify if you...
- Mentally disabled or significantly altered mental status that would prevent understanding and giving informed consent
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 10 years
Participants who undergo fertility preserving cancer treatment are observed to record cancer diagnosis, treatment, and outcomes including fertility and oncologic results.
Periodic visits as part of routine cancer care
Trial Site Locations
Total: 2 locations
1
UZ Gasthuisberg, Katholieke Universiteit Leuven
Leuven, Belgium, 3000
Actively Recruiting
2
The Netherlands Cancer Institute - Antoni van Leeuwenhoek Hospital
Amsterdam, Netherlands
Actively Recruiting
Research Team
K
Katrien Van Tornout
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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