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Apply Biphasic IVM for POSEIDON Group 1 (POSEIDON-Ia)

2 giugno 2026 aggiornato da: Mỹ Đức Hospital

Efficacy and Safety of Biphasic IVM in Low Prognosis Patients Classified as Poseidon Group 1A

The goal of this clinical trial is to learn if biphasic In Vitro Maturation (IVM) works to help young women who produce very few oocytes after controlled ovarian stimulation. The study focuses on women under age 35 who have a good number of follicles in their ovaries but do not respond well to standard ovarian stimulation by Gonadotropin (known as POSEIDON Group 1a).

The main questions it aims to answer are:

How many mature oocytes can be obtain after biphasic -VM? Researchers will use biphasic-IVM system to see if it can bypass the problems these patients face with standard treatments, such as high costs and the risk of medical complications like Ovarian Hyperstimulation Syndrome (OHSS).

Participants will:

Have their immature eggs collected from the ovaries without the need for high-dose hormone injections.

Have their eggs matured in a specialized laboratory using a two-step process (biphasic IVM) to improve egg quality.

Follow up with researchers to check the number of embryos created and the safety of the procedure.

Panoramica dello studio

Stato

Non ancora reclutamento

Intervento / Trattamento

Descrizione dettagliata

In assisted reproductive technology (ART), patients with poor or suboptimal ovarian response to controlled ovarian hyperstimulation pose significant clinical challenges, leading to the development of the POSEIDON classification in 2016. In particular, POSEIDON group 1a includes young patients (under 35 years of age) with normal ovarian reserve parameters (AFC ≥5 and/or AMH ≥1.2 ng/mL) who nevertheless have a low number of retrieved oocytes (<4 oocytes) following standard ovarian stimulation (Humaidan et al., 2016). The cause of this is often attributed to genetic factors, such as FSH receptor (FSHR) or LH receptor (LHR) polymorphisms, leading to ovarian resistance or reduced sensitivity to exogenous gonadotropins." (Alviggi et al., 2018). Current traditional IVF treatment strategies for this group typically focus on increasing gonadotropin dosages, adding recombinant LH, or applying double stimulation protocols (DuoStim) to maximize the number of oocytes retrieved and obtain at least one euploid blastocyst. However, these approaches not only substantially increase treatment costs and the psychological burden on patients, but may also elevate the risk of ovarian hyperstimulation syndrome (OHSS) due to the presence of a high number of antral follicles. Moreover, their true effectiveness remains controversial, as the pathophysiology is related to reduced receptor sensitivity rather than a simple hormonal deficiency (Haahr et al., 2018; Conforti et al., 2019).

The application of biphasic IVM in POSEIDON group 1 patients represents a biologically and clinically rational strategy. This technique leverages the advantage of preserved ovarian reserve (a high number of small follicles) to retrieve immature oocytes without relying on high-dose gonadotropin stimulation, thereby bypassing receptor resistance mechanisms. In addition, it nearly eliminates the risk of OHSS and reduces treatment costs (Grynberg et al., 2021). Previous studies investigating IVM in patients with poor ovarian response mainly focused on rescuing immature oocytes retrieved during conventional stimulation cycles (rescue-IVM) to increase embryo availability. However, pregnancy outcomes derived from rescue-IVM have generally been low (Elias et al., 2014; Herrero et al., 2018; Kushnir et al., 2018).

Biphasic IVM offers a promising alternative approach. This protocol includes a prematuration phase using C-type Natriuretic Peptide (CNP) to temporarily arrest meiotic progression for 24 hours, thereby restoring synchronization between nuclear and cytoplasmic maturation, followed by a 30-hour maturation phase. This strategy significantly improves oocyte developmental competence and blastocyst formation rates (Sanchez et al., 2019; Vuong et al., 2020). The aim of this study is to evaluate the efficacy and safety of biphasic IVM in patients classified as POSEIDON Group 1a.

Tipo di studio

Interventistico

Iscrizione (Stimato)

25

Fase

  • Non applicabile

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Contatto studio

Backup dei contatti dello studio

Luoghi di studio

    • Hồ Chí Minh
      • Ho Chi Minh City, Hồ Chí Minh, Vietnam, 70000

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Adulto

Accetta volontari sani

No

Descrizione

Inclusion Criteria:

  • Women aged 18 - < 35 years
  • At least one IVF cycle have been failed and classified as having a poor response to POSEIDON group Ia.
  • POSEIDON group Ia ( < 35 age; AMH >= 1.2 ng/ml and/or AFC >=5 antral follicles; have < 4 oocytes was retrieved at previous IVF cycle)
  • Agree to apply biphasic-IVM treatment.
  • Agree to freeze all embryos and to transfer the frozen embryos afterward.
  • Agree to participate in the study.

Exclusion Criteria:

  • Egg-donation cycle
  • Uterine abnormalities: adenomyosis, large uterine fibroids (≥5 cm), bicornuate uterus, uterine adhesions.
  • Sperm surgical (PESA, TESE, mTESE)

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Trattamento
  • Assegnazione: N / A
  • Modello interventistico: Assegnazione di gruppo singolo
  • Mascheramento: Nessuno (etichetta aperta)

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: Biphasic-IVM
Participants in this arm will undergo a biphasic In Vitro Maturation (IVM) protocol

After consenting to undergo biphasic IVM, patients will be scheduled for immature oocyte retrieval between cycle days 1 and 6. No FSH, hMG, hCG, or GnRH agonist will be administered for oocyte maturation. Oocyte retrieval will be performed transvaginally under ultrasound guidance. A 20G aspiration needle (Kitazato®, Japan or Vitrolife®, Sweden) will be connected to a suction device with a negative pressure of -120 mmHg.

Follicular fluid will be transferred to the laboratory for oocyte identification under a stereomicroscope and filtered using a mesh system to avoid oocyte loss. Cumulus-oocyte complexes (COCs) will be washed and placed into four-well culture dishes containing CAPA medium. After 24 hours of prematuration culture in CAPA medium, the oocytes will be transferred to IVM medium for an additional 30 hours. Subsequently, oocytes will be denuded and assessed for nuclear maturation status. Mature oocytes obtained after IVM culture will undergo intracytoplasmic sperm injection.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Number of matured oocytes after biphasic-IVM
Lasso di tempo: From enrollment to the last of treatment at 12 months
Count the number of oocytes with the first polar body extruded after biphasic IVM culture
From enrollment to the last of treatment at 12 months

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Number of patients have no oocyte retrieved
Lasso di tempo: From enrollment to the last of treatment at 12 months
Count the number of patients with no oocytes retrieved
From enrollment to the last of treatment at 12 months
Number of patients have no matured oocytes after biphasic IVM
Lasso di tempo: From enrollment to the last of treatment at 12 months
Count the number of patients with no matured oocytes after biphasic IVM
From enrollment to the last of treatment at 12 months
Number of patients have no embryos
Lasso di tempo: From enrollment to the end of treatment at 12 months
Count the number of patients with no embryos
From enrollment to the end of treatment at 12 months
Recovery rate
Lasso di tempo: From enrollment to the end of treatment at 12 months
Number of GV oocytes/number of follicles
From enrollment to the end of treatment at 12 months
Maturation rate
Lasso di tempo: From enrollment to the end of treatment at 12 month
Number of matured oocytes after biphasic-IVM/number of GV oocytes
From enrollment to the end of treatment at 12 month
Number of fertilized oocytes
Lasso di tempo: From enrollment to the last of treatment at 12 months
Number of 2PN oocytes after ICSI 16 - 18 hours
From enrollment to the last of treatment at 12 months
Number of embryos day-3 oocytes
Lasso di tempo: From enrollment to the last of treatment at 12 months
Number of cleavage embryos after ICSI 64 hours
From enrollment to the last of treatment at 12 months
Day-3 embryos rate
Lasso di tempo: From enrollment to the last of treatment at 12 months
Number of day-3 embryos/number of 2PN
From enrollment to the last of treatment at 12 months
Number of good embryos day-3
Lasso di tempo: From enrollment to the last of treatment at 12 months
Mean number of usable embryos day-3
From enrollment to the last of treatment at 12 months
Number of frozen embryos day-3
Lasso di tempo: From enrollment to the last of treatment at 12 months
Mean number of Day-3 cryopreserved embryos
From enrollment to the last of treatment at 12 months
Number of blastocyst embryos
Lasso di tempo: From enrollment to the last of treatment at 12 months
Mean number of Day-5 embryos
From enrollment to the last of treatment at 12 months
Blastocyst rate
Lasso di tempo: From enrollment to the last of treatment at 12 months
Number of blastocyst/ number of 2 PN
From enrollment to the last of treatment at 12 months
Number of good blastocyst embryos
Lasso di tempo: From enrollment to the last of treatment at 12 months
Mean number of usable blastocyts embryos
From enrollment to the last of treatment at 12 months
Number of frozen blastocyst embryos
Lasso di tempo: From enrollment to the last of treatment at 12 months
Mean number of Day-5 cryopreserved embryos
From enrollment to the last of treatment at 12 months
Pregnancy rate
Lasso di tempo: From enrollment to the last of treatment at 12 months
Serum beta-hCG level > 25 mIU/ml after transfer 11 - 13 days
From enrollment to the last of treatment at 12 months
Implantion rate
Lasso di tempo: From enrollment to the last of treatment at 12 months
Number of visible gestational sac (included ectopic pregnancy)/ number of embryos transferred
From enrollment to the last of treatment at 12 months
Clinical pregnancy rate
Lasso di tempo: From enrollment to the end of treatment at 12 months
At least one gestational sac was observed on ultrasound at 7 gestational weeks
From enrollment to the end of treatment at 12 months
Ongoing pregnancy rate
Lasso di tempo: From enrollment to the end of treatment at 12 moths
At least one fetus with heart beat was observed on ultrasound at 12 gestational weeks
From enrollment to the end of treatment at 12 moths
Live birth rate
Lasso di tempo: From enrollment to the end of treatment at 12 moths
The complete expulsion or extraction of a product of human conception from its mother irrespective of pregnancy duration which, after separation, breathes or shows any sign of life, such as a beating heart, umbilical cord pulsation, or voluntary muscle movement
From enrollment to the end of treatment at 12 moths
Ectopic pregnancy rate
Lasso di tempo: From enrollment to the end of treatment at 12 months
Percentage of patients with ectopic pregnancy
From enrollment to the end of treatment at 12 months
Miscarriage rate < 12 gestational weeks
Lasso di tempo: From enrollment to the end of treatment at 12 months
Percentage of patients with miscarriage pregnancy < 12 weeks
From enrollment to the end of treatment at 12 months
Multiple pregnancy rate
Lasso di tempo: From enrollment to the end of treatment at 12 months
Percentage of patients with multiple pregnancy (> 1 gestational sac)
From enrollment to the end of treatment at 12 months
OHSS rate
Lasso di tempo: From enrollment to the end of treatment at 12 months
Percentage of patients with OHSS requiring hospitalization
From enrollment to the end of treatment at 12 months
Internal bleeding after OPU
Lasso di tempo: From enrollment to the end of treatment at 12 months
Percentage of patients with internal bleeding after OPU requiring hospitalization
From enrollment to the end of treatment at 12 months
Fertilization rate
Lasso di tempo: From enrollment to the end of treatment at 12 months
Number of 2PN/ Number of MII
From enrollment to the end of treatment at 12 months

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Investigatori

  • Investigatore principale: Ho L. Le, MD

Pubblicazioni e link utili

La persona responsabile dell'inserimento delle informazioni sullo studio fornisce volontariamente queste pubblicazioni. Questi possono riguardare qualsiasi cosa relativa allo studio.

Pubblicazioni generali

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Stimato)

1 giugno 2026

Completamento primario (Stimato)

30 dicembre 2026

Completamento dello studio (Stimato)

30 marzo 2027

Date di iscrizione allo studio

Primo inviato

2 giugno 2026

Primo inviato che soddisfa i criteri di controllo qualità

2 giugno 2026

Primo Inserito (Effettivo)

8 giugno 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

8 giugno 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

2 giugno 2026

Ultimo verificato

1 giugno 2026

Maggiori informazioni

Termini relativi a questo studio

Altri numeri di identificazione dello studio

  • 07/26/DD-BVMD

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

NO

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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