Flushing technique may boost egg retrieval in women with low ovarian reserve
NCT ID NCT01329302
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tested whether flushing follicles with a special needle during egg retrieval helps women who produce few eggs in IVF. 257 women with fewer than 5 mature follicles were randomly assigned to standard aspiration or aspiration plus flushing. The goal was to see if flushing increases the number of mature eggs collected and improves pregnancy rates.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Follicular flushing with double lumen needle
- What this could lead to
- If successful, this technique could help women with low ovarian response retrieve more eggs during IVF, potentially increasing their chances of pregnancy.
- What could go wrong
- This is a completed study with 257 participants, but the benefit may be small and not apply to all patients. Flushing adds time and cost to the procedure.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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257 people
The number who actually took part.
- Started
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Mar 2011
- Finished
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Jun 2016
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 43 years
- Sex
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Female participants only
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * 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 Exclusion Criteria: * 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
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Centre d'Assistance Médicale à la Procréation, CMCO-SIHCUS
Schiltigheim, Schiltigheim, 67300, France
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