N/A
N=29
Investigational Oocyte Cryopreservation for Medical and Non Medical Indications
Infertility, Female · Deferred Childbearing
Bottom Line
View on ClinicalTrials.gov: NCT04616417 ↗Enrolled (actual)
29
Serious AEs
0.0%
Results posted
Jul 2024
Primary outcome: Primary: Fertility Quality of Life Questionnaire Completed After One Year After Oocyte Cryopreservation for Non-medical Reasons — 9 Participants
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Investigational Oocyte Cryopreservation (Procedure)
- Age
- Adult · 18+ yrs
- Sex
- Female
- Sponsor
- University of Illinois at Chicago
- Primary completion
- Mar 2023
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Fertility Quality of Life Questionnaire Completed After One Year After Oocyte Cryopreservation for Non-medical Reasons |
9 | — |
| PRIMARY Structured Clinical Interview Completed After One Year After Oocyte Cryopreservation for Non-medical Reasons |
9 | — |
| PRIMARY Fertility Quality of Life Questionnaire Completed After One Year After Oocyte Cryopreservation for Cancer Patients |
1 | — |
| PRIMARY Structured Clinical Interview Completed After One Year After Oocyte Cryopreservation for Cancer Patients |
1 | — |
Summary
This is a prospective study to assess the long term benefits and outcomes of the existing oocyte cryopreservation methods for fertility preservation in women with a potential medical or non medical risk of loss of fertility
Eligibility Criteria
Inclusion Criteria
- Women aged >18 and 10 mIU/ml for patients having egg freezing for a medical indication
- Serum FSH > 10 mIU/ml for patients having egg freezing for social reasons
- Women with psychological, psychiatric, or other conditions which prevent giving fully informed consent (Post Traumatic Stress Disorder, severe depression, bipolar disorder, schizophrenia, severe anxiety and inability to cope)
- Patients with extensive disease whose therapy is deemed palliative by the medical oncologist
Data sourced from ClinicalTrials.gov (NCT04616417). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.