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Long-term Evaluation of Fertility Preservation Options in Women in Cancer Remission or Haematological Pathology

Long-term Evaluation of Fertility Preservation Options in Women in Cancer Remission or Haematological Pathology

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07312058
Acronym
FERT-ISSUES
Enrollment
102
Registered
2025-12-31
Start date
2025-12-17
Completion date
2027-01-01
Last updated
2026-01-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Assisted Reproductive Technology, Cancer Remission, Female Cancer Survivors, Fertility Counseling, Fertility Observatory, Fertility Preservation, Fertility Preservation Techniques, Live Birth Rate, Oncology, Patient Follow-up, Psychological Impact, Reproductive Health, Reproductive Outcomes

Keywords

Fertility preservation, Cancer remission, Reproductive outcomes, Reproductive health, Oncology, Fertility counseling, Assisted reproductive technology, Psychological impact, Fertility observatory, Patient follow-up, Female cancer survivors, Fertility preservation techniques, Live birth rate

Brief summary

Cancer treatments, despite their increasing effectiveness, carry a significant risk of gamete toxicity. Women of reproductive age are commonly offered fertility preservation (FP) before starting their treatment. However, few studies have analyzed the long-term reproductive outcomes of these interventions, nor how patients ultimately use or do not use the FP options once in remission. This project aims to better understand the effectiveness, utilization, and psychological impacts of these strategies. This work is part of an effort to understand and evaluate fertility preservation practices implemented for women of reproductive age undergoing cancer treatment at the Amiens-Picardie University Hospital (CHU). Its objective is to document patient pathways, clinical decisions, techniques employed, and reproductive outcomes observed after remission, in order to identify potential areas for improvement in the support and follow-up of these patients, thereby enhancing the overall quality and coordination of care. This work is conducted alongside the development of a fertility observatory at the Department of Medicine and Reproductive Biology, CHU Amiens-Picardie.

Interventions

None listed

Sponsors

Centre Hospitalier Universitaire, Amiens
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 47 Years
Healthy volunteers
No

Inclusion criteria

* Women * Aged between 18 and 47 years * Diagnosed with cancer or hematological disorders requiring potentially gonadotoxic treatment * Having undergone a medical fertility preservation consultation * Followed at Amiens Picardie University Hospital (CHU Amiens Picardie) in the department of Reproductive Medicine * Currently in remission * Having expressed non-opposition to participation in the study

Exclusion criteria

* Absence of remission * Patients deprived of liberty by administrative or judicial decision, or placed under legal protection (guardianship or curators) * Decline to participate in the study

Design outcomes

Primary

MeasureTime frameDescription
Occurrence of an identifiable reproductive outcome1 yearIdentifiable reproductive outcome are Spontaneous pregnancy, Use of preserved gametes or ovarian tissue (whether or not resulting in pregnancy), Use of donor oocytes, Discontinuation of the parenthood project

Secondary

MeasureTime frameDescription
Type of fertility preservation method performed1 year
Time interval (in months) between diagnosis and fertility preservation1 year
Correlation between Age and occurance of an identifiable reproductive outcome1 yearIdentifiable reproductive outcome are Spontaneous pregnancy, Use of preserved gametes or ovarian tissue (whether or not resulting in pregnancy), Use of donor oocytes, Discontinuation of the parenthood project
Time interval (in months) between fertility preservation and initiation of potentially gonadotoxic treatment1 year
Number of type of cancer associated with identifiable reproductive outcome1 yearIdentifiable reproductive outcome are Spontaneous pregnancy, Use of preserved gametes or ovarian tissue (whether or not resulting in pregnancy), Use of donor oocytes, Discontinuation of the parenthood project
Correlation between type of treatment and occurence of an identifiable reproductive outcome1 yearIdentifiable reproductive outcome are Spontaneous pregnancy, Use of preserved gametes or ovarian tissue (whether or not resulting in pregnancy), Use of donor oocytes, Discontinuation of the parenthood project
Correlation between family status and occurence of an identifiable reproductive outcome1 yearIdentifiable reproductive outcome are Spontaneous pregnancy, Use of preserved gametes or ovarian tissue (whether or not resulting in pregnancy), Use of donor oocytes, Discontinuation of the parenthood project
Time interval (in months) between completion of treatment and pregnancy attempt (spontaneous or medically assisted)1 year
Actual utilization rate of preserved material1 year
Success rate of reuse attempts1 year
Proportion of patients who ultimately did not pursue parenthood1 year

Countries

France

Contacts

CONTACTCABRY-GOUBET Rosalie, Pr
cabry.rosalie@chu-amiens.fr33+3 22 08 80 00

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026