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Constitution of a Cohort for Monitoring Patients Candidating for Ovarian Tissue Autograft

Constitution of a Cohort for Monitoring Patients Candidating for Ovarian Tissue Autograft

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02855827
Acronym
PERIDATOR
Enrollment
240
Registered
2016-08-04
Start date
2013-05-31
Completion date
2025-10-31
Last updated
2024-07-12

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

Conditions

Ovarian Function Insufficiency

Brief summary

Ovarian cryopreservation is one of the available option for preserving fertility prior to potentially sterilizing treatments. In the absence of other techniques such as in vitro folliculogenesis or injection of isolated ovarian follicles, this tissue can only be re-used by autograft. In France, the first live birth after orthotopic ovarian transplantation, was obtained by Roux et al. in 2009. This clinical trial aims to build a cohort of patients likely to use their ovarian tissue cryopreserved by autograft.

Detailed description

Ovarian cryopreservation is one of the available option for preserving fertility prior to potentially sterilizing treatments. In the absence of other techniques such as in vitro folliculogenesis or injection of isolated ovarian follicles, this tissue can only be re-used by autograft. In France, the first live birth after orthotopic ovarian transplantation, was obtained by Roux et al. in 2009. This clinical trial aims to build a cohort of patients likely to use their ovarian tissue cryopreserved by autograft. This cohort will be used to: * Follow up of patients with their cryopreserved ovarian tissue; * Evaluate requests for ovarian tissue grafting ; * Propose a search of residual disease in case of neoplastic disease risk (if possible); * Allowing patients to benefit from an ovarian tissue autograft; * Assess the effectiveness of autograft technique after the restoration of ovarian function.

Interventions

None listed

Sponsors

CHU de Reims
CollaboratorOTHER
University Hospital, Marseille
CollaboratorOTHER
University Hospital, Lille
CollaboratorOTHER
Central Hospital, Nancy, France
CollaboratorOTHER
University Hospital, Grenoble
CollaboratorOTHER
CMCO SIHCUS, Schiltingheim
CollaboratorOTHER
University Hospital, Bordeaux
CollaboratorOTHER
Nantes University Hospital
CollaboratorOTHER
University Hospital, Limoges
CollaboratorOTHER
Centre Hospitalier Universitaire de Besancon
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
OTHER

Eligibility

Sex/Gender
FEMALE
Age
11 Years to 43 Years
Healthy volunteers
No

Inclusion criteria

* Patients who have cryopreserved their ovarian tissue; * Patients with premature ovarian insufficiency; * Patients older than 11 years (bone age) for induction of puberty; * Patients aged from 18 to 43 years for the restoration of ovarian function; * No objection from the patient * Patients who have already received ovarian tissue autograft.

Exclusion criteria

* Patients aged under 11 years (bone age); * Patients older than 43 years; * Patients refusing to be included; * Patients (adults) under guardianship, curators and safeguard justice

Design outcomes

Primary

MeasureTime frame
Number of patient who are candidate to ovarian tissue autograft5 years

Countries

France

Contacts

Primary ContactChlotilde AMIOT, MD, PhD
camiot@chu-besancon.fr

Outcome results

None listed

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