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CancerPTONCT03674164

Fertility Preservation With Ovarian Tissue Freezing

A study testing Ovarian Cryopreservation in people with Cancer and Hematologic Disorder, run by St. Justine's Hospital at 1 site in Canada.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

The purpose of this study is to obtain ovarian tissue from female patients undergoing gonadotoxic treatments or gonadal ablating surgery, and that in consequence may see their future fertility impaired. Read more about this study

Who is it for?
Ages 2 months to 18 years, women only
Conditions the study is for
Cancer, Hematologic Disorder, Infertility
What is being tested?
Ovarian Cryopreservation
How many people
250 participants
Where
1 siteCanada
Study dates
10 Sep 2019to 31 Dec 2023
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 2 months to 18 years
  • Women only
  • No healthy volunteers
  • Child, Adult

Who may be able to join

  • Females, > 2 month and < 18 years of age
  • Undergo surgery, chemotherapy, drug treatment, and/or radiation for the treatment or prevention of a medical condition or malignancy expected to result in permanent and complete loss of subsequent ovarian function.
  • Or, have a medical condition or malignancy that requires removal of all or part of one or both ovaries.
  • Subject may have newly diagnosed or recurrent disease.
  • Subject who already has stored cryopreserved ovarian tissue in a frozen state prior to undergoing cancer treatments (surgery, chemotherapy or radiation) will be eligible for enrolment with informed consent.
  • Subject not eligible to standard fertility preservation
  • The subject and/or the subject's legally authorized guardian must acknowledge in writing that consent for specimen collection has been obtained, in accordance with institutional policies.

Who cannot join

  • Women with psychological, psychiatric or other conditions which prevent giving fully informed consent.
  • Women whose underlying medical condition significantly increases their risk of complications from anesthesia and surgery.
  • Women to whom the research intervention may decrease the survival or the treatment response to the underlying disease.
  • AMH (Anti Müllerian Hormone) <0.016 ng/dl
  • Women whose surgery is preformed outside the CHU Ste-Justine
  • Patients eligible to a standard fertility preservation procedure.
  • -

Trial locations and contacts

1 site in 1 country.

Canada1 site
  • CHU Ste-Justine

    Montreal, Quebec, H3X 1C6

    Julio Saumet Chilito, MD, 5143454931 ext. 6323, julio.saumet.chilito@umontreal.ca

    Pascal Desrosier, BSC, 5143454931 ext. 6323, pascal.des.rosiers.hsj@ssss.gouv.qc.ca

Other trials in Canada

About this study

The purpose of this study is to obtain ovarian tissue from female patients undergoing gonadotoxic treatments or gonadal ablating surgery, and that in consequence may see their future fertility impaired. Participants will be offered to preserve (freeze) and use ovarian tissue for the purpose of conceiving in the future.

Although, 86 live births have been reported with ovarian tissue cryo-preservation and grafting, the procedure is still considered experimental.

This research, will help us to learn and validate how to perform ovarian tissue cryo-preservation and thawing in the fertility preservation context.

Read the detailed description

his Study will conducted at the Centre Hospitalier Universitaire Ste-Justine Collected ovarian tissue will only be for the patients own use.

Subjects will undergo surgical removal of their ovarian tissue, and the following categories will be invited to participate:

  1. Patients have elected to have one or both ovaries removed for the treatment or prevention of disease.
  2. Patients who have elected to have surgery to remove all or part of one or both ovaries for medical reasons where cryopreservation of the remaining limited portions of normal ovarian cortex is the only option for fertility preservation at the time (except that ovarian cortex from the ovary that contains the mass will not be cryopreserved).
  3. Participants who have elected to have one or part of one ovary removed, solely for the purpose of fertility preservation because they are not candies to use standard fertility preservation technologies.

If the subject chooses to participate and consent, she will be assessed to determine her eligibility The subject will also have a serum AMH drawn for the evaluation of the ovarian reserve, and also infectious disease testing will also be performed per Health Canada guidelines.

The oophorectomie will be performed laparoscopically under general anesthesia. In patients' in whom it is medically unsafe or not feasible to complete the surgery laparoscopically, the patient and/or legal gardian may opt to proceed with a mini-laparotomy or laparotomy approach or may opt to stop the procedure and withdraw from the study at that time. This decision will be discussed with the patient and legal gardian during the consenting process and documented prior to the surgery. The procedural risk and treatment delays will be discussed with the primary treatment team in order to provide a better evaluation of the patients wellbeing. This procedure is performed for fertility preservation purposes only, but can potentially be coordinated with another procedure such as placement of a central line for future chemotherapy. In the event the subject is undergoing a surgical intervention for other indications, the oophorectomies could be coordinated at the same time.

A tissu sample will be evaluated by pathology for routine histologic evaluation. If the pathologist finds evidence of neoplasia in the ovarian tissue sample. All the tissue could be send to pathology for a more detailed examination. In this case, there will be no tissue available for the subject to use for fertility preservation.

Cryopreservation :

Ovarian tissue preparation:

  1. Ovarian tissue will be transported from the operating room at the CHU Sainte-Justine to the Embryology laboratory at the REI department in a modified HTF supplemented with 10% supplement serum substitute (9922 SSS; Irvine Scientifc, Santa Ana, CA, USA) and deposed in a heated trait at 37 °C.
  2. The ovarian cortex will be separated from the medulla and cut in tissue bands (0.5-1 x 0.5- 1cm, 1-2 mm)
  3. Tissue washing with TCM 199 (Life technologies, Foster City, CA, USA) supplemented with 20% (v/v) SSS (milieu WS) and then exposed to three different vitrification solutions at room temperature.

Vitrification:

  1. Ovarian tissue equilibration in TCM199 avec 10% (v/v) ethylene glycol (EG, Wako Pure Chemical Industries, Tokyo, Japan) et 20% (v/v) SSS for 5 minutes.
  2. Ovarian tissue equilibration in TCM199 with 20%(v/v) EG and 20% (v/v) SSS for 5 minutes.
  3. Ovarian tissue equilibration in TCM199 avec 35%(v/v) EG, 5% (w/v) polyvinylpyrrolidone (sigma-Aldrich, St. Louis, MO, USA) et 0.5 mol/l sucrose (Wako Pure Chemical industries) for 5 minutes.
  4. Ovarian tissue bands will be installed on" Cryosupport " (BD Bioscience, San Jose, CA, USA) before immersion in liquid nitrogen.
  5. Ovarian tissue bands will be stored in a cryo vial at -196°C.

The ovarian tissue bio-bank is located at the embryology laboratory in the REI department at the CHU Ste-Justine

Infectious disease screening:

As per Health Canada guidelines, patients will be screened for (VIH, VDRL, HBsAg, anti Hepatitis C, HTLV).

Study and safety data collection:

Adverse events after an elective oophorectomy will be identified according to the Health Canada criteria (www.hc-sc.gc.ca/ahc-asc/media/advisories-avis/reaction-eng.php#Drugs).

Data Collection :

  1. Date of fertility preservation
  2. Intervention type
  3. Age
  4. Age at diagnosis
  5. Age at menarche
  6. Diagnosis
  7. Outcome: remission, relapse, or death
  8. Gynaecological history
  9. Obstetrical and neonatal outcomes
  10. Treatment regimen associated with high risk of sterility
  11. Choices regarding use of cryopreserved stored tissue for fertility restoration Fertility preservation outcome

Risks:

The potential risks of laparoscopy, laparotomy, and oophorectomy include injury to bowel, bladder, and blood vessels with need for subsequent repair. The chance of the subject requiring hospitalization for complication(s) is about 1%. In addition to the surgical risk, there are also inherent risks of general anesthesia. The subject's chance of dying from anesthesia is less than 1 in 10,000. The risk of injury with laparotomy is moderate. The subject, legal guardian, and/or parent(s) will be asked to sign the standard consent form for laparoscopy, and/or laparotomy and oophorectomy after the risks and benefits have been discussed. The subject, legal guardian(s), and/or parent(s) will also be asked by the anesthesiology team to sign an anesthesia consent form after risks and benefits have been discussed.

There is a risk that the ovary to be cryopreserved may be affected by cancer, disqualifying the subject from ovarian tissue freezing. Although care will be taken, damage to the removed ovarian tissue may occur during any part of the cryopreservation, shipping or storage process. The effects of cryopreservation and long term storage on human ovarian tissues are not known and possible damage to the tissues may occur; in this instance a future pregnancy may not occur. The birth defect(s) and/or genetic damage to any child who may be born following ovarian tissue cryopreservation procedure are also unknown. However, thousands of children have been born worldwide from frozen embryos and eggs and there has been no report of increased risk of birth defects in these children.

Benefits:

The patient participation in the study protocol may provide her with a means to restore her fertility and reproductive hormonal function. However, However, there is a significant possibility that there may be no direct benefit due to no utilization of the ovarian tissue, or that the ovarian tissue may not result in any live brith.

Costs: All expenses related to this procedure will be covered by the "Régie s'Assurance du Québec". Tissue storage is also covered for a period of five years.

Being tested
Ovarian Cryopreservation
Medical subject headings
Neoplasms, Hematologic Diseases, Infertility

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Ovarian CryopreservationOther

    Surgical ovarian removal and vitrification

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Cryopreservation of ovarian tissu by vitrification

    Measure the fertility rate of cryopreservation and grafting by ovarian tissue vitrification.

    Measured: 5 years

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted17 Sep 2018
  2. Study start10 Sep 2019 (estimated)
  3. Primary completion31 Dec 2023 (estimated)
  4. Study completion31 Dec 2023 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Other
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
250 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT03674164
Sponsor's protocol ID
217-1341
Acronym
PTO
Status last verified
Sep 2018
First submitted
13 Sep 2018
Last updated
17 Sep 2018
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing Ovarian Cryopreservation in people with Cancer and Hematologic Disorder, run by St. Justine's Hospital at 1 site in Canada.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 7 inclusion and 7 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 17 Sep 2018. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Canada. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

Contact Julio Saumet Chilito, MD (5143454931 ext. 6323, julio.saumet.chilito@umontreal.ca), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Cryopreservation of ovarian tissu by vitrification (time frame: 5 years). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 17 Sep 2018.

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