Follicular Activation in Poor Responders (FAPPOR)
Primary Purpose
Infertility
Status
Unknown status
Phase
Not Applicable
Locations
Spain
Study Type
Interventional
Intervention
In vitro fragmentation of the ovarian tissue
Sponsored by
About this trial
This is an interventional treatment trial for Infertility focused on measuring Poor ovarian response, Salvador/Warts/Hippo pathway, Follicular activation, Poor ovarian reserve
Eligibility Criteria
Inclusion Criteria (must meet one):
- At least two episodes of poor ovarian response (≤ 3 oocytes retrieved with a standard protocol).
- A previous IVF cycle with ≤ 3 oocytes (following a standard stimulation protocol) and presence of an abnormal ovarian reserve test (antral follicle count of ≤ 5 or antimüllerian hormone ≤ 5pm).
Exclusion Criteria (must not meet any):
- Patients under 18 or over 40 years.
- Clinical signs of endometriosis.
- Previous ovarian surgery.
- Genital tract malformations.
- Anovulatory patient (defined by the presence of irregular cycles and serum progesterone ≤ 10 ng / mL on cycle day 21).
- Partner with severe male factor: severe oligoasthenozoospermia, oligoasthenoteratozoospermia and azoospermia.
- All those patients who do not voluntarily give their express written consent.
Sites / Locations
- La Fe University HospitalRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
No Intervention
Experimental
Arm Label
Control arm
Experimental arm
Arm Description
No intervention is performed. Assessment of antral follicle count. IVF treatment.
Perform intervention described: Laparoscopy. In vitro fragmentation of the ovarian tissue. Assessment of antral follicle count. IVF treatment.
Outcomes
Primary Outcome Measures
Antral follicle count
Secondary Outcome Measures
Full Information
NCT ID
NCT02354963
First Posted
January 22, 2015
Last Updated
November 17, 2016
Sponsor
Instituto de Investigacion Sanitaria La Fe
1. Study Identification
Unique Protocol Identification Number
NCT02354963
Brief Title
Follicular Activation in Poor Responders
Acronym
FAPPOR
Official Title
Follicle Activation in Patients With Poor Ovarian Response Through Fragmentation of the Ovarian Tissue.
Study Type
Interventional
2. Study Status
Record Verification Date
September 2016
Overall Recruitment Status
Unknown status
Study Start Date
November 2014 (undefined)
Primary Completion Date
June 2017 (Anticipated)
Study Completion Date
December 2017 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Instituto de Investigacion Sanitaria La Fe
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
This study aims to assess whether activation of primordial follicles through ovarian cortex fragmentation may increase the number of antral follicles present in the ovary of patients with diminished ovarian reserve. Secondary outcomes include number of oocytes retrieved and pregnancy rates after IVF.
Hypothesis; Evaluate whether the proposed intervention increases the pool of antral follicles (potentially stimulable ones).
Detailed Description
Controlled, randomized, assessor-blind clinical trial.
Thirty-six patients of La Fe University Hospital (Valencia), previously confirmed as poor responders according to the European Society of Human Reproduction and Embryology (ESHRE) criteria, will be randomized to two treatment arms:
Arm 1 (control): no intervention.
Arm 2 (intervention): ovarian cortex extraction by unilateral laparoscopic biopsy and ovarian tissue fragmentation in aliquots of 1 mm2. These fragments will be grafted under the ovarian cortex and meso-ovarium ipsilateraly.
Subsequently the number of antral follicles in both intervention groups will be compared and also will be the number of antral follicles in the native ovary and the grafted one in each of the patients.
Patients will receive a standard IVF treatment for poor responders according to the protocols of the assisted reproduction unit of La Fe University Hospital.
The final aim is to assess the pregnancy rate in both groups, as well as parameters related to the reproduction technique when required.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Infertility
Keywords
Poor ovarian response, Salvador/Warts/Hippo pathway, Follicular activation, Poor ovarian reserve
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
36 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Control arm
Arm Type
No Intervention
Arm Description
No intervention is performed. Assessment of antral follicle count. IVF treatment.
Arm Title
Experimental arm
Arm Type
Experimental
Arm Description
Perform intervention described: Laparoscopy. In vitro fragmentation of the ovarian tissue.
Assessment of antral follicle count. IVF treatment.
Intervention Type
Procedure
Intervention Name(s)
In vitro fragmentation of the ovarian tissue
Intervention Description
Unilateral ovarian cortex extraction, in vitro fragmentation and reimplantation.
Primary Outcome Measure Information:
Title
Antral follicle count
Time Frame
Up to 6 months
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria (must meet one):
At least two episodes of poor ovarian response (≤ 3 oocytes retrieved with a standard protocol).
A previous IVF cycle with ≤ 3 oocytes (following a standard stimulation protocol) and presence of an abnormal ovarian reserve test (antral follicle count of ≤ 5 or antimüllerian hormone ≤ 5pm).
Exclusion Criteria (must not meet any):
Patients under 18 or over 40 years.
Clinical signs of endometriosis.
Previous ovarian surgery.
Genital tract malformations.
Anovulatory patient (defined by the presence of irregular cycles and serum progesterone ≤ 10 ng / mL on cycle day 21).
Partner with severe male factor: severe oligoasthenozoospermia, oligoasthenoteratozoospermia and azoospermia.
All those patients who do not voluntarily give their express written consent.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Cesar Diaz-Garcia, MD
Email
cesar.diaz@uv.es
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Cesar Diaz-Garcia, MD
Organizational Affiliation
La Fe University Hospital. University of Valencia
Official's Role
Principal Investigator
Facility Information:
Facility Name
La Fe University Hospital
City
Valencia
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
César Díaz García
Phone
+34618830870
Email
cesar.diaz@uv.es
First Name & Middle Initial & Last Name & Degree
Carlos Simón Vallés
First Name & Middle Initial & Last Name & Degree
Antonio Pellicer Martínez
First Name & Middle Initial & Last Name & Degree
Sonia Herraiz Raya
First Name & Middle Initial & Last Name & Degree
Loida Pamplona Bueno
First Name & Middle Initial & Last Name & Degree
Natalia Fischer Suárez
12. IPD Sharing Statement
Citations:
PubMed Identifier
35367015
Citation
Diaz-Garcia C, Herraiz S, Pamplona L, Subira J, Soriano MJ, Simon C, Seli E, Pellicer A. Follicular activation in women previously diagnosed with poor ovarian response: a randomized, controlled trial. Fertil Steril. 2022 Apr;117(4):747-755. doi: 10.1016/j.fertnstert.2021.12.034.
Results Reference
derived
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Follicular Activation in Poor Responders
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