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

2026년 6월 2일 업데이트: 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.

연구 개요

상태

아직 모집하지 않음

개입 / 치료

상세 설명

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.

연구 유형

중재적

등록 (추정된)

25

단계

  • 해당 없음

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 연락처

연구 연락처 백업

연구 장소

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

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

  • 성인

건강한 자원 봉사자를 받아들입니다

아니

설명

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)

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

  • 주 목적: 치료
  • 할당: 해당 없음
  • 중재 모델: 단일 그룹 할당
  • 마스킹: 없음(오픈 라벨)

무기와 개입

참가자 그룹 / 팔
개입 / 치료
실험적: 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.

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Number of matured oocytes after biphasic-IVM
기간: 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

2차 결과 측정

결과 측정
측정값 설명
기간
Number of patients have no oocyte retrieved
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

수사관

  • 수석 연구원: Ho L. Le, MD

간행물 및 유용한 링크

연구에 대한 정보 입력을 담당하는 사람이 자발적으로 이러한 간행물을 제공합니다. 이것은 연구와 관련된 모든 것에 관한 것일 수 있습니다.

일반 간행물

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작 (추정된)

2026년 6월 1일

기본 완료 (추정된)

2026년 12월 30일

연구 완료 (추정된)

2027년 3월 30일

연구 등록 날짜

최초 제출

2026년 6월 2일

QC 기준을 충족하는 최초 제출

2026년 6월 2일

처음 게시됨 (실제)

2026년 6월 8일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2026년 6월 8일

QC 기준을 충족하는 마지막 업데이트 제출

2026년 6월 2일

마지막으로 확인됨

2026년 6월 1일

추가 정보

이 연구와 관련된 용어

기타 연구 ID 번호

  • 07/26/DD-BVMD

개별 참가자 데이터(IPD) 계획

개별 참가자 데이터(IPD)를 공유할 계획입니까?

아니요

약물 및 장치 정보, 연구 문서

미국 FDA 규제 의약품 연구

아니

미국 FDA 규제 기기 제품 연구

아니

이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .

건강한 성인 여성에 대한 임상 시험

Biphasic-IVM에 대한 임상 시험

구독하다