Infertility (IVF Patients)FOFLORNCT07335016
The Role of Follicular Flushing at Oocyte Retrieval
A study testing follicular flushing and Simple aspiration in people with Infertility (IVF Patients) and Oocyte Retrieval for IVF, run by Aristotle University Of Thessaloniki at 2 sites in Greece.
Trial summary
In vitro fertilization (IVF) is the most common method of medically assisted reproduction, involving fertilization of the egg by sperm in a lab. The process includes ovarian stimulation, oocyte retrieval, fertilization and culture, and embryo transfer. Read more about this study
- Who is it for?
- Ages 18 to 46 years, women only
- Conditions the study is for
- Infertility (IVF Patients), Oocyte Retrieval for IVF
- What is being tested?
- follicular flushing and Simple aspiration
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 75 participants
- Where
- 2 sitesGreece
- Study dates
- 14 Jan 2026to 20 Jan 2029
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
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 18 to 46 years
- Women only
- No healthy volunteers
- Adult
Who may be able to join
- Ovarian stimulation with recFSH and GnRH antagonist or PPOS protocol
- Triggering final oocyte maturation with hCG or GnRH agonist
- The day of oocyte retrieval at least one follicle of mean diameter of 11mm in each ovary
- ICSI method of fertilisation.
Who cannot join
- Presence of ovarian cyst of endometriosis
- History of ovarian surgery
- Monofollicular growth
- Presence of only one ovary
- Ovary not accessible at oocyte retrieval
Trial locations and contacts
2 sites in 1 country. Contact the study team or a site near you to ask about taking part.
Greece2 sites
Eugonia IVF
Athens
Georgios Lainas, +306979333999, g.lainas@yahoo.co.uk
Georgios Lainas
Aristotle University of Thessaloniki
Thessaloniki
Efstratios Kolibianakis, Professor, +306937096078, stratis.kolibianakis@gmail.com
Theoni Tarlatzi, +306945853581, nonika.tarlatzi@gmail.com
About this study
In vitro fertilization (IVF) is the most common method of medically assisted reproduction, involving fertilization of the egg by sperm in a lab. The process includes ovarian stimulation, oocyte retrieval, fertilization and culture, and embryo transfer. The success of IVF depends mainly on female age-as age increases, ovarian reserve and oocyte quality decrease-and the number of oocytes retrieved.
This study investigates whether follicular flushing during oocyte retrieval can increase the number of mature oocytes retrieved. This randomized study will be conducted in women undergoing ovarian stimulation with recombinant Folicullar Stimulating Hormone (FSH) and Gonadotropin-Releasing Hormone (GnRH) antagonist or Progestin Primed Ovarian Stimulation (PPOS) to suppress premature Luteinizing hormone (LH) rise. Final oocyte maturation will be triggered with recombinant Human chorionic gonadotropin (hCG) or GnRH agonist.
Read more
Eligible participants will have at least one follicle ≥11 mm in each ovary. On the day of oocyte retrieval, one ovary will be randomized to undergo follicular flushing using a single-lumen needle and the other simple aspiration, using the same needle. All fertilized oocytes from both ovaries will be cultured, seperately, to the blastocyst stage.
Study outcomes are the number of oocytes and mature oocytes retrieved, the oocyte retrieval rate, the mature oocyte retrieval rate, the maturation rate, the number of fertilized oocytes, the fertilisation rate, the number of blastocytes and the blastulation rate.
Sample size of 75 patients (25 per response category: poor, normal, high) provides 82-98% power to detect clinically meaningful interaction effects (Cohen's f=0.19-0.34) between response category and technique (follicular flushing vs. simple aspiration) under conservative assumptions of 50-70% of pilot study effects, lower correlations (ρ=0.35), and increased variability (α=0.05, two-sided, 5% attrition buffer.
Read the detailed description
In vitro fertilization (IVF) is the most commonly applied method of medically assisted reproduction and concerns the fertilization of the egg by the sperm in a laboratory environment. The process includes the following stages: Ovarian stimulation, oocyte retrieval, fertilization and culture in the laboratory, and finally, embryo transfer.
Achieving pregnancy and live birth depends on several factors. The most important is the woman's age, as the advanced female reproductive age reduces the ovarian reserve and increases the chromosomal abnormalities of the remaining oocytes. The other important factor is the number of oocytes retrieved.
Follicular flushing aims to increase the number of mature oocytes retrieved at oocyte retrieval. The present thesis investigates the role of follicular flushing at oocyte retrieval.
The randomized study will be conducted in women undergoing ovarian stimulation with recombinant follicle-stimulating hormone (recFSH) and suppression of the premature rise of luteinizing hormone (LH) using a gonadotropin-releasing hormone (GnRH) antagonist or Progestin Primed Ovarian Stimulation (PPOS). Induction of final oocyte maturation will be done with recombinant human chorionic gonadotropin (rec hCG) or an agonist of GnRH.
Women with at least one follicle of a mean diameter of 11 millimetres or more in each ovary will be eligible to participate in the studies.
On the day of oocyte retrieval, one ovary will be randomized to undergo follicular flushing using a single-lumen needle and the other simple aspiration, using the same needle. All fertilized oocytes from both ovaries will be cultured, seperately, to the blastocyst stage.
The outcomes are the number of oocytes and mature oocytes retrieved during oocyte retrieval, the oocyte retrieval rate, the mature oocyte retrieval rate, the maturation rate, the number of fertilized oocytes, the fertilisation rate, the number of blastocytes and the blastulation rate.
This study requires 75 patients (25 per response category: poor, normal, high responders) to rigorously evaluate whether follicular flushing with single-lumen needles produces clinically meaningful improvements in oocyte yield. We employed multiple conservative assumptions to ensure adequate power even under pessimistic scenarios.
Sample size was calculated for a mixed-design ANOVA testing the Response × Technique interaction. Our published pilot study (Lainas et al., HR, 2023, N=105) using double-lumen needles demonstrated large effects, but we conservatively assume single-lumen needles will show only 50-70% of these effects. We further assumed: (1) within-ovary correlations of ρ=0.35 (lower than pilot's 0.44-0.59), (2) standard deviations 20% higher than pilot data, and (3) 90% power requirement (vs. standard 80%).
Under these ultra-conservative assumptions (50% of pilot effects), n=25 per group provides 82% power. For more realistic scenarios (70-80% of pilot effects), power exceeds 90-98%. This sample size accommodates 5% attrition (target enrollment N=79), which is appropriate for within-ovary designs where dropout is minimal. The conservative approach ensures the study can detect meaningful clinical differences while satisfying rigorous peer review standards and protecting against optimistic assumptions about equipment transition.
- Being tested
- follicular flushing, Simple aspiration
- Keywords
- ivf, follicular flushing, oocyte retrieval
- Medical subject headings
- Infertility, Long Qt Syndrome 3
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
follicular flushingOther
Follicular flushing in IVF is a technique used during oocyte retrieval with the aim to increase the number of oocytes retrieved. In follicular flushing, after the initial aspiration, the follicle is rinsed (flushed) with a sterile fluid using the same needle. In the first arm, follicular flushing will be performed in the left ovary.
Simple aspirationOther
Simple aspiration in IVF is the technique used during oocyte retrieval to retrieve the oocytes from the ovaries.
| Study group | Role | What they receive |
|---|---|---|
| Follicular flushing | Active comparator | Follicular flushing Receives: Other: follicular flushing |
| Simple aspiration | Active comparator | Simple aspiration Receives: Other: Simple aspiration |
What is being measured
The primary outcome is the main question the study is designed to answer.
Number of oocytes retrieved
Oocytes retrieved at oocyte retrieval are collected in the laboratory
Measured: Day 0
Secondary outcomes (8)
Number of mature oocytes retrieved
Maturity of oocytes retrieved is observed in the laboratory about 2 hours after oocyte retrieval
Measured: Day 0
Oocyte retrieval rate
Oocytes retrieved per mature follicles observed at the ultrasound on the day of trigger of oocyte maturation
Measured: Day 0
Mature oocyte retrieval rate
Mature oocytes per number of mature follicles at the trigger of oocyte maturation
Measured: Day 0
Rate of mature oocytes / total number of oocytes retrieved
Rate of mature oocytes per total number of oocytes retrieved
Measured: Day 0
Number of fertilized oocytes
Fertilisation is observed one day after the ICSI method
Measured: Day 1
Rate of fertilized oocytes / total number of mature oocytes retrieved
Rate of fertilized oocytes per total number of mature oocytes retrieved
Measured: Day 1
Number of blastocysts
Number of blastocysts formed from the fertilised oocytes
Measured: Day 5 and Day 6
Rate of blastocysts/total number of fertilized oocytes
Rate of blastocysts formed per total number of fertilized oocytes
Measured: Day 5 and Day 6
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted12 Jan 2026
- Study start14 Jan 2026 (estimated)
- Primary completion15 Jan 2028 (estimated)
- Study completion20 Jan 2029 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for Infertility (IVF Patients)Studies of the same condition, open and under way.
- More trials run by Aristotle University Of ThessalonikiThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Model description
- This study design, where each patient undergoing IVF has one ovary randomized to follicular flushing and the contralateral ovary to simple aspiration, is classified as a parallel intervention study model with within-participant (or split-body) randomization at the organ level.
- Masking
- None (open label)
- Enrolment
- 75 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Aristotle University Of Thessaloniki
- Sponsor type
- University, hospital or other
- Collaborators
- Eugonia IVF Unit, Athens, Greece
- Responsible party
- Principal investigator, E.M. Kolibianakis, Aristotle University Of Thessaloniki
- Investigators
- Efstratios Kolibianakis, Professor, Principal investigator, Unit of Human Reproduction, Aristotle University of Thessaloniki
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07335016
- Sponsor's protocol ID
- UHR-18
- Acronym
- FOFLOR
- Status last verified
- Jan 2026
- First submitted
- 17 Nov 2025
- Last updated
- 13 Jan 2026
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Undecided
Publications
Lainas GT, Lainas TG, Makris AA, Xenariou MV, Petsas GK, Kolibianakis EM. Follicular flushing increases the number of oocytes retrieved: a randomized controlled trial. Hum Reprod. 2023 Oct 3;38(10):1927-1937. doi: 10.1093/humrep/dead169.
PubMed 37632249
Study at a glance
From the registry record, last updated by the sponsor on 13 Jan 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- The Role of Follicular Flushing at Oocyte Retrieval
- ClinicalTrials.gov ID
- NCT07335016
- Acronym / sponsor ID
- FOFLOR / UHR-18
- Keywords
- ivf, follicular flushing, oocyte retrieval
- Study type
- Interventional
- Recruitment status
- Not yet recruiting
- Enrolment
- 75 participants (estimated)
- Lead sponsor
- Aristotle University Of ThessalonikiUniversity, hospital or other
- Collaborators
- Eugonia IVF Unit, Athens, Greece
- Study start
- 14 Jan 2026 (estimated)
- Primary completion
- 15 Jan 2028 (estimated)
- Study completion
- 20 Jan 2029 (estimated)
- First posted
- 12 Jan 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
In vitro fertilization (IVF) is the most common method of medically assisted reproduction, involving fertilization of the egg by sperm in a lab. The process includes ovarian stimulation, oocyte retrieval, fertilization and culture, and embryo transfer. The success of IVF depends mainly on female age-as age increases, ovarian reserve and oocyte quality decrease-and the number of oocytes retrieved.
This study investigates whether follicular flushing during oocyte retrieval can increase the number of mature oocytes retrieved. This randomized study will be conducted in women undergoing ovarian stimulation with recombinant Folicullar Stimulating Hormone (FSH) and Gonadotropin-Releasing Hormone (GnRH) antagonist or Progestin Primed Ovarian Stimulation (PPOS) to suppress premature Luteinizing hormone (LH) rise. Final oocyte maturation will be triggered with recombinant Human chorionic gonadotropin (hCG) or GnRH agonist.
Eligible participants will have at least one follicle ≥11 mm in each ovary. On the day of oocyte retrieval, one ovary will be randomized to undergo follicular flushing using a single-lumen needle and the other simple aspiration, using the same needle. All fertilized oocytes from both ovaries will be cultured, seperately, to the blastocyst stage.
Study outcomes are the number of oocytes and mature oocytes retrieved, the oocyte retrieval rate, the mature oocyte retrieval rate, the maturation rate, the number of fertilized oocytes, the fertilisation rate, the number of blastocytes and the blastulation rate.
Sample size of 75 patients (25 per response category: poor, normal, high) provides 82-98% power to detect clinically meaningful interaction effects (Cohen's f=0.19-0.34) between response category and technique (follicular flushing vs. simple aspiration) under conservative assumptions of 50-70% of pilot study effects, lower correlations (ρ=0.35), and increased variability (α=0.05, two-sided, 5% attrition buffer.
Detailed description
In vitro fertilization (IVF) is the most commonly applied method of medically assisted reproduction and concerns the fertilization of the egg by the sperm in a laboratory environment. The process includes the following stages: Ovarian stimulation, oocyte retrieval, fertilization and culture in the laboratory, and finally, embryo transfer.
Achieving pregnancy and live birth depends on several factors. The most important is the woman's age, as the advanced female reproductive age reduces the ovarian reserve and increases the chromosomal abnormalities of the remaining oocytes. The other important factor is the number of oocytes retrieved.
Follicular flushing aims to increase the number of mature oocytes retrieved at oocyte retrieval. The present thesis investigates the role of follicular flushing at oocyte retrieval.
The randomized study will be conducted in women undergoing ovarian stimulation with recombinant follicle-stimulating hormone (recFSH) and suppression of the premature rise of luteinizing hormone (LH) using a gonadotropin-releasing hormone (GnRH) antagonist or Progestin Primed Ovarian Stimulation (PPOS). Induction of final oocyte maturation will be done with recombinant human chorionic gonadotropin (rec hCG) or an agonist of GnRH.
Women with at least one follicle of a mean diameter of 11 millimetres or more in each ovary will be eligible to participate in the studies.
On the day of oocyte retrieval, one ovary will be randomized to undergo follicular flushing using a single-lumen needle and the other simple aspiration, using the same needle. All fertilized oocytes from both ovaries will be cultured, seperately, to the blastocyst stage.
The outcomes are the number of oocytes and mature oocytes retrieved during oocyte retrieval, the oocyte retrieval rate, the mature oocyte retrieval rate, the maturation rate, the number of fertilized oocytes, the fertilisation rate, the number of blastocytes and the blastulation rate.
This study requires 75 patients (25 per response category: poor, normal, high responders) to rigorously evaluate whether follicular flushing with single-lumen needles produces clinically meaningful improvements in oocyte yield. We employed multiple conservative assumptions to ensure adequate power even under pessimistic scenarios.
Sample size was calculated for a mixed-design ANOVA testing the Response × Technique interaction. Our published pilot study (Lainas et al., HR, 2023, N=105) using double-lumen needles demonstrated large effects, but we conservatively assume single-lumen needles will show only 50-70% of these effects. We further assumed: (1) within-ovary correlations of ρ=0.35 (lower than pilot's 0.44-0.59), (2) standard deviations 20% higher than pilot data, and (3) 90% power requirement (vs. standard 80%).
Under these ultra-conservative assumptions (50% of pilot effects), n=25 per group provides 82% power. For more realistic scenarios (70-80% of pilot effects), power exceeds 90-98%. This sample size accommodates 5% attrition (target enrollment N=79), which is appropriate for within-ovary designs where dropout is minimal. The conservative approach ensures the study can detect meaningful clinical differences while satisfying rigorous peer review standards and protecting against optimistic assumptions about equipment transition.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
- Model description
- This study design, where each patient undergoing IVF has one ovary randomized to follicular flushing and the contralateral ovary to simple aspiration, is classified as a parallel intervention study model with within-participant (or split-body) randomization at the organ level.
| Arm | Type | Receives |
|---|---|---|
| Follicular flushing | Active comparator | Other: follicular flushingFollicular flushing |
| Simple aspiration | Active comparator | Other: Simple aspirationSimple aspiration |
Who may qualify
- Ages
- 18 to 46 years
- Sex
- Female only
- Healthy volunteers
- Not accepted
- Age groups
- Adult
Key inclusion criteria (4 listed)
- Ovarian stimulation with recFSH and GnRH antagonist or PPOS protocol
- Triggering final oocyte maturation with hCG or GnRH agonist
- The day of oocyte retrieval at least one follicle of mean diameter of 11mm in each ovary
- ICSI method of fertilisation.
Key exclusion criteria (5 listed)
- Presence of ovarian cyst of endometriosis
- History of ovarian surgery
- Monofollicular growth
- Presence of only one ovary
- Ovary not accessible at oocyte retrieval
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| follicular flushingFollicular flushing in IVF is a technique used during oocyte retrieval with the aim to increase the number of oocytes retrieved. In follicular flushing, after the initial aspiration, the follicle is rinsed (flushed) with a sterile fluid using the same needle. In the first arm, follicular flushing will be performed in the left ovary. | Other | Follicular flushing |
| Simple aspirationSimple aspiration in IVF is the technique used during oocyte retrieval to retrieve the oocytes from the ovaries. | Other | Simple aspiration |
Primary outcome
Number of oocytes retrieved
Time frame: Day 0
Oocytes retrieved at oocyte retrieval are collected in the laboratory
8 secondary outcomes
Number of mature oocytes retrieved
Time frame: Day 0
Oocyte retrieval rate
Time frame: Day 0
Mature oocyte retrieval rate
Time frame: Day 0
Rate of mature oocytes / total number of oocytes retrieved
Time frame: Day 0
Number of fertilized oocytes
Time frame: Day 1
Rate of fertilized oocytes / total number of mature oocytes retrieved
Time frame: Day 1
Number of blastocysts
Time frame: Day 5 and Day 6
Rate of blastocysts/total number of fertilized oocytes
Time frame: Day 5 and Day 6
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 13 Jan 2026.
- Background: PubMed 37632249Lainas GT, Lainas TG, Makris AA, Xenariou MV, Petsas GK, Kolibianakis EM. Follicular flushing increases the number of oocytes retrieved: a randomized controlled trial. Hum Reprod. 2023 Oct 3;38(10):1927-1937. doi: 10.1093/humrep/dead169.
- Individual participant dataSharing planned: Undecided
Related trials for Infertility (IVF Patients)
RecruitingObservational study
Pilot Study of Discarded Blastocysts
Infertility (IVF Patients)
Active, not recruitingPhase 3
Human Menopausal Gonadotropin Research in Infertility Assessing Cumulative Live Birth With Frozen Embryo Transfer.
Infertility (IVF Patients)
Recruiting
225 IU Versus 300 IU Starting FSH Dose in PPOS for Good-Prognosis Women
Infertility (IVF Patients), Infertility Assisted Reproductive Technology
Recruiting
The Effects of Carnitine Supplementation on Oocytes in Women Undergoing IVF Process
Infertility (IVF Patients)
Not yet recruiting
Intra-ovarian CAPA-IVM vs Standard IVM
Infertility (IVF Patients), Infertility
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Efstratios Kolibianakis, Professor principal investigator
Unit of Human Reproduction, Aristotle University of Thessaloniki
2 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing follicular flushing and Simple aspiration in people with Infertility (IVF Patients) and Oocyte Retrieval for IVF, run by Aristotle University Of Thessaloniki at 2 sites in Greece.
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 4 inclusion and 5 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: opening soon, as of the sponsor's last update on 13 Jan 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 2 sites in Greece. 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?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Efstratios Prof. Kolibianakis (+306937096078, stratis.kolibianakis@gmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Number of oocytes retrieved (time frame: Day 0). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT07335016, which also lists 1 linked publication.
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 13 Jan 2026.