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

2. Juni 2026 aktualisiert von: 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.

Studienübersicht

Status

Noch keine Rekrutierung

Intervention / Behandlung

Detaillierte Beschreibung

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.

Studientyp

Interventionell

Einschreibung (Geschätzt)

25

Phase

  • Unzutreffend

Kontakte und Standorte

Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.

Studienkontakt

Studieren Sie die Kontaktsicherung

Studienorte

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

Teilnahmekriterien

Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.

Zulassungskriterien

Studienberechtigtes Alter

  • Erwachsene

Akzeptiert gesunde Freiwillige

Nein

Beschreibung

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)

Studienplan

Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.

Wie ist die Studie aufgebaut?

Designdetails

  • Hauptzweck: Behandlung
  • Zuteilung: N / A
  • Interventionsmodell: Einzelgruppenzuweisung
  • Maskierung: Keine (Offenes Etikett)

Waffen und Interventionen

Teilnehmergruppe / Arm
Intervention / Behandlung
Experimental: 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.

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Number of matured oocytes after biphasic-IVM
Zeitfenster: 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

Sekundäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Number of patients have no oocyte retrieved
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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

Mitarbeiter und Ermittler

Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.

Ermittler

  • Hauptermittler: Ho L. Le, MD

Publikationen und hilfreiche Links

Die Bereitstellung dieser Publikationen erfolgt freiwillig durch die für die Eingabe von Informationen über die Studie verantwortliche Person. Diese können sich auf alles beziehen, was mit dem Studium zu tun hat.

Allgemeine Veröffentlichungen

Studienaufzeichnungsdaten

Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.

Haupttermine studieren

Studienbeginn (Geschätzt)

1. Juni 2026

Primärer Abschluss (Geschätzt)

30. Dezember 2026

Studienabschluss (Geschätzt)

30. März 2027

Studienanmeldedaten

Zuerst eingereicht

2. Juni 2026

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

2. Juni 2026

Zuerst gepostet (Tatsächlich)

8. Juni 2026

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Tatsächlich)

8. Juni 2026

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

2. Juni 2026

Zuletzt verifiziert

1. Juni 2026

Mehr Informationen

Begriffe im Zusammenhang mit dieser Studie

Andere Studien-ID-Nummern

  • 07/26/DD-BVMD

Plan für individuelle Teilnehmerdaten (IPD)

Planen Sie, individuelle Teilnehmerdaten (IPD) zu teilen?

NEIN

Arzneimittel- und Geräteinformationen, Studienunterlagen

Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt

Nein

Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt

Nein

Diese Informationen wurden ohne Änderungen direkt von der Website clinicaltrials.gov abgerufen. Wenn Sie Ihre Studiendaten ändern, entfernen oder aktualisieren möchten, wenden Sie sich bitte an register@clinicaltrials.gov. Sobald eine Änderung auf clinicaltrials.gov implementiert wird, wird diese automatisch auch auf unserer Website aktualisiert .

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