Benefit of Follicular Flushing During Oocyte Retrieval for Poor Responder Patient in an Assisted Reproductive Technology Program
Follicular Flushing for Poor Responder Patient in an Assisted Reproductive Technology Program: Flush Study
1 other identifier
interventional
257
1 country
1
Brief Summary
The object of this study is to determine the benefit of follicular flushing with a double channel needle in a poor responder population for a maximum number of oocytes to be retrieved. The investigators compare two methods of oocyte retrieval with or without flushing. 220 patients undergoing an in vitro fertilization (IVF) or Intracytoplasmic Sperm Injection (ICSI) have to be included. All patients with less than 5 follicles of 14 mm and more the day of ovulation induction will be included, following a randomized protocol in two groups, Group A: Oocyte retrieval is performed with a single lumen aspiration needle 17G. Group B: Oocyte retrieval is performed with a double lumen aspiration needle 17G. all follicles are flushed with flushing solution in addition to direct aspiration of the follicular fluid, 20CC of flushing medium is provided for all the procedure and flushing medium is collected separately from direct fluid aspiration in order to follow up each oocyte one by one. First criterion of our comparison is the number of oocyte retrieved. Second criteria are: oocyte quality, fertilization rate, number and quality of embryos obtained, clinical pregnancy rate. In Group B the investigators will compare two subgroups: oocytes collected in flush medium and oocytes from direct follicle fluid. Then the investigators will know the capability of oocyte collected after follicular flushing to be fertilized and to increase the success chance of pregnancy for poor responder patients.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Mar 2011
Longer than P75 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
December 22, 2010
CompletedStudy Start
First participant enrolled
March 1, 2011
CompletedFirst Posted
Study publicly available on registry
April 5, 2011
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 1, 2016
CompletedStudy Completion
Last participant's last visit for all outcomes
June 1, 2016
CompletedDecember 16, 2025
December 1, 2025
5.3 years
December 22, 2010
December 15, 2025
Conditions
Outcome Measures
Primary Outcomes (2)
the number of mature oocytes collected
Increase the number of mature oocytes collected during the follicular flushing with a double lumen aspiration needle
2 years and 9 months
quality of embryos obtained
Embryo quality is assessed at the Laboratory of Reproductive Biology by a score based on: cell number, cell regularity and degree of fragmentation.
2 years and 9 months
Secondary Outcomes (3)
Number of embryos obtained
2 years and 9 months
Number of transferable embryos (transferred and frozen)
2 years and 9 months
Number of pregnancies obtained
2 years and 9 months
Study Arms (2)
Group A: Direct aspiration
ACTIVE COMPARATORFollicular Flushing
ACTIVE COMPARATORInterventions
In addition to direct aspiration of the follicular fluid all follicles are flushed with flushing solution, 20CC of flushing medium( Flushing Medium MediCultâ France) is provided for all the procedure and flushing medium is collected separately from direct fluid
Eligibility Criteria
You may qualify if:
- patients undergoing an IVF or ICSI treatment
- long agonist, antagonist or short stimulations protocols
- less than 5 follicles of 14mm or more day of HCG
- Major patients aged under 43 years
- patient within a couple married or can prove a married life of over 2 years
You may not qualify if:
- all the cons indication to the oocyte retrieval
- oocyte donor
- Couple supported viral loop
- Patient does not speak French or unable to give informed consent
- Patients major protected
- Patients with biopsy performed on weekends are also excluded due to unavailability of adequate personnel and equipment
- Absence of follicles
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Centre d'Assistance Médicale à la Procréation, CMCO-SIHCUS
Schiltigheim, Schiltigheim, 67300, France
Related Publications (1)
Calabre C, Schuller E, Goltzene MA, Rongieres C, Celebi C, Meyer N, Teletin M, Pirrello O. Follicular flushing versus direct aspiration in poor responder IVF patients: a randomized prospective study. Eur J Obstet Gynecol Reprod Biol. 2020 May;248:118-122. doi: 10.1016/j.ejogrb.2020.03.003. Epub 2020 Mar 6.
PMID: 32200248RESULT
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- CARE PROVIDER
- Purpose
- OTHER
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
December 22, 2010
First Posted
April 5, 2011
Study Start
March 1, 2011
Primary Completion
June 1, 2016
Study Completion
June 1, 2016
Last Updated
December 16, 2025
Record last verified: 2025-12