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Combined Ovarian Tissue and Oocyte Cryopreservation for Fertility

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Summary

NIH ClinicalTrials.gov registered observational study NCT07546123 will compare combined ovarian tissue cryopreservation with oocyte cryopreservation against oocyte cryopreservation alone in oncological patients undergoing gonadotoxic treatments. The study will collect data from two groups of patients assigned based on their planned gonadotoxic therapy and available time before treatment initiation. The primary endpoints are the number of oocytes retrieved per ovarian stimulation cycle and the oocyte retrieval rate between the two groups.

“Combining ovarian tissue cryopreservation followed by oocyte cryopreservation may maximize fertility preservation by safeguarding more follicles and ensuring availability of mature oocytes.”

NIH , verbatim from source
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GovPing monitors ClinicalTrials.gov Studies for new healthcare & life sciences regulatory changes. Every update since tracking began is archived, classified, and available as free RSS or email alerts — 686 changes logged to date.

What changed

NIH ClinicalTrials.gov registered an observational study comparing combined ovarian tissue cryopreservation followed by oocyte cryopreservation against oocyte cryopreservation alone for fertility preservation in oncological patients. Patients will be assigned to treatment groups based on their planned gonadotoxic therapy and available time before treatment initiation. The study will compare oocytes retrieved per stimulation cycle and oocyte retrieval rates between the two groups.

Healthcare providers and clinical investigators involved in fertility preservation services for cancer patients may benefit from awareness of this comparative data collection, which may inform clinical practice and patient counseling regarding cryopreservation options.

Archived snapshot

Apr 22, 2026

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Ovarian Tissue Cryopreservation Combined With Oocyte Cryopreservation Versus Oocyte Cryopreservation Alone

Observational NCT07546123 Kind: OBSERVATIONAL Apr 22, 2026

Abstract

Fertility preservation is a crucial aspect of care for oncological patients undergoing gonadotoxic treatments such as chemotherapy, radiotherapy, or surgery, which can significantly reduce ovarian reserve and cause infertility or premature menopause. Among available techniques, oocyte cryopreservation is well-established with high survival rates but requires controlled ovarian stimulation and may not be suitable for prepubertal patients or those needing urgent cancer therapy. Ovarian tissue cryopreservation offers advantages by preserving a larger number of primordial follicles, can be performed anytime in the menstrual cycle regardless of age, and also helps restore ovarian endocrine function.

Combining ovarian tissue cryopreservation followed by oocyte cryopreservation may maximize fertility preservation by safeguarding more follicles and ensuring availability of mature oocytes.

This study will collect data from two patient groups:

Group 1: patients undergoing ovarian tissue cryopreservation followed by oocyte cryopreservation (combined treatment)

Group 2: patients undergoing oocyte cryopreservation alone.

Group assignment is based on planned gonadotoxic therapy and available time before treatment initiation, according to clinical practice.

The study aims to compare the number of oocytes retrieved per ovarian stimulation cycle between the two groups, along with the oocyte retrieval rate (number of oocytes retrieved/number of aspirated follicles), number of mature o...

Conditions: Oncological Disease, Fertility Preservation

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Last updated

Classification

Agency
NIH
Instrument
Notice
Branch
Executive
Legal weight
Non-binding
Stage
Final
Change scope
Minor
Document ID
NCT07546123

Who this affects

Applies to
Clinical investigators Healthcare providers
Industry sector
6211 Healthcare Providers
Activity scope
Fertility preservation procedures Clinical trial conduct
Geographic scope
United States US

Taxonomy

Primary area
Healthcare
Operational domain
Clinical Operations
Topics
Healthcare Pharmaceuticals

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