- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT07632300
Apply Biphasic IVM for POSEIDON Group 1 (POSEIDON-Ia)
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
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
등록 (추정된)
단계
- 해당 없음
연락처 및 위치
연구 연락처
- 이름: Tuong M Ho, MD
- 전화번호: +84903633377
- 이메일: tuongho.ivfmd@gmail.com
연구 연락처 백업
- 이름: Ho L. Le, MD
- 전화번호: +84356177147
- 이메일: bsho.ll@myduchospital.vn
연구 장소
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Hồ Chí Minh
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Ho Chi Minh City, Hồ Chí Minh, 베트남, 70000
- IVFMD, My Duc Hospital
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연락하다:
- Ho L. Le, MD
- 전화번호: 84356177147
- 이메일: bsho.ll@myduchospital.vn
-
-
참여기준
자격 기준
공부할 수 있는 나이
- 성인
건강한 자원 봉사자를 받아들입니다
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
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
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From enrollment to the last of treatment at 12 months
|
2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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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
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From enrollment to the last of treatment at 12 months
|
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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
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From enrollment to the last of treatment at 12 months
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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
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From enrollment to the end of treatment at 12 months
|
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Recovery rate
기간: From enrollment to the end of treatment at 12 months
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Number of GV oocytes/number of follicles
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From enrollment to the end of treatment at 12 months
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Maturation rate
기간: From enrollment to the end of treatment at 12 month
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Number of matured oocytes after biphasic-IVM/number of GV oocytes
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From enrollment to the end of treatment at 12 month
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Number of fertilized oocytes
기간: From enrollment to the last of treatment at 12 months
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Number of 2PN oocytes after ICSI 16 - 18 hours
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From enrollment to the last of treatment at 12 months
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Number of embryos day-3 oocytes
기간: From enrollment to the last of treatment at 12 months
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Number of cleavage embryos after ICSI 64 hours
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From enrollment to the last of treatment at 12 months
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Day-3 embryos rate
기간: From enrollment to the last of treatment at 12 months
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Number of day-3 embryos/number of 2PN
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From enrollment to the last of treatment at 12 months
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Number of good embryos day-3
기간: From enrollment to the last of treatment at 12 months
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Mean number of usable embryos day-3
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From enrollment to the last of treatment at 12 months
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Number of frozen embryos day-3
기간: From enrollment to the last of treatment at 12 months
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Mean number of Day-3 cryopreserved embryos
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From enrollment to the last of treatment at 12 months
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Number of blastocyst embryos
기간: From enrollment to the last of treatment at 12 months
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Mean number of Day-5 embryos
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From enrollment to the last of treatment at 12 months
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Blastocyst rate
기간: From enrollment to the last of treatment at 12 months
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Number of blastocyst/ number of 2 PN
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From enrollment to the last of treatment at 12 months
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Number of good blastocyst embryos
기간: From enrollment to the last of treatment at 12 months
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Mean number of usable blastocyts embryos
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From enrollment to the last of treatment at 12 months
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Number of frozen blastocyst embryos
기간: From enrollment to the last of treatment at 12 months
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Mean number of Day-5 cryopreserved embryos
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From enrollment to the last of treatment at 12 months
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Pregnancy rate
기간: From enrollment to the last of treatment at 12 months
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Serum beta-hCG level > 25 mIU/ml after transfer 11 - 13 days
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From enrollment to the last of treatment at 12 months
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Implantion rate
기간: From enrollment to the last of treatment at 12 months
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Number of visible gestational sac (included ectopic pregnancy)/ number of embryos transferred
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From enrollment to the last of treatment at 12 months
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Clinical pregnancy rate
기간: From enrollment to the end of treatment at 12 months
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At least one gestational sac was observed on ultrasound at 7 gestational weeks
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From enrollment to the end of treatment at 12 months
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Ongoing pregnancy rate
기간: From enrollment to the end of treatment at 12 moths
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At least one fetus with heart beat was observed on ultrasound at 12 gestational weeks
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From enrollment to the end of treatment at 12 moths
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Live birth rate
기간: From enrollment to the end of treatment at 12 moths
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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
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From enrollment to the end of treatment at 12 moths
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Ectopic pregnancy rate
기간: From enrollment to the end of treatment at 12 months
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Percentage of patients with ectopic pregnancy
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From enrollment to the end of treatment at 12 months
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Miscarriage rate < 12 gestational weeks
기간: From enrollment to the end of treatment at 12 months
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Percentage of patients with miscarriage pregnancy < 12 weeks
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From enrollment to the end of treatment at 12 months
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Multiple pregnancy rate
기간: From enrollment to the end of treatment at 12 months
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Percentage of patients with multiple pregnancy (> 1 gestational sac)
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From enrollment to the end of treatment at 12 months
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OHSS rate
기간: From enrollment to the end of treatment at 12 months
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Percentage of patients with OHSS requiring hospitalization
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From enrollment to the end of treatment at 12 months
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Internal bleeding after OPU
기간: From enrollment to the end of treatment at 12 months
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Percentage of patients with internal bleeding after OPU requiring hospitalization
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From enrollment to the end of treatment at 12 months
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Fertilization rate
기간: From enrollment to the end of treatment at 12 months
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Number of 2PN/ Number of MII
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From enrollment to the end of treatment at 12 months
|
공동 작업자 및 조사자
스폰서
수사관
- 수석 연구원: Ho L. Le, MD
간행물 및 유용한 링크
일반 간행물
- Yalcinkaya E, Caliskan E, Budak O. In vitro maturation may prevent the cancellation of in vitro fertilization cycles in poor responder patients: A case report. J Turk Ger Gynecol Assoc. 2013 Jul 10;14(4):235-7. doi: 10.5152/jtgga.2013.68335. eCollection 2013.
- Alviggi C, Conforti A, Esteves SC, Vallone R, Venturella R, Staiano S, Castaldo E, Andersen CY, De Placido G. Understanding Ovarian Hypo-Response to Exogenous Gonadotropin in Ovarian Stimulation and Its New Proposed Marker-The Follicle-To-Oocyte (FOI) Index. Front Endocrinol (Lausanne). 2018 Oct 17;9:589. doi: 10.3389/fendo.2018.00589. eCollection 2018.
- Conforti A, Esteves SC, Di Rella F, Strina I, De Rosa P, Fiorenza A, Zullo F, De Placido G, Alviggi C. The role of recombinant LH in women with hypo-response to controlled ovarian stimulation: a systematic review and meta-analysis. Reprod Biol Endocrinol. 2019 Feb 6;17(1):18. doi: 10.1186/s12958-019-0460-4.
- Haahr T, Esteves SC, Humaidan P. Individualized controlled ovarian stimulation in expected poor-responders: an update. Reprod Biol Endocrinol. 2018 Mar 9;16(1):20. doi: 10.1186/s12958-018-0342-1.
- Grynberg, M. and Fanchin, R. (2021) 'IVM in non-PCOS indications', in In Vitro Maturation of Human Oocytes. CRC Press.
- Herrero, L., Pareja, S., Losada, C. and Cobo, A. (2018) 'In vitro maturation (IVM) for patients with poor ovarian response: a pilot study', Journal of Clinical Medicine, 7(12), p. 524.
- Humaidan, P., Alviggi, C., Fischer, R. and Esteves, S.C. (2016) 'The 'POSEIDON' stratification of 'Low Prognosis Patients in Assisted Reproductive Technology': we can stop looking for the ideal patient', Human Reproduction, 31(10), pp. 2201-2211.
- Kushnir, V.A., Gleicher, N., Barad, D.H. and Albertini, D.F. (2018) 'A single-center study of in vitro maturation in patients with low ovarian reserve', Journal of Ovarian Research, 11(1), pp. 1-6.
- Sanchez, F., Leuzinger, L., Romero, S., De Vos, M., Heindryckx, B. and Smitz, J. (2019) 'In vitro maturation with a prematuration step (CAPA-IVM) improves the meiotic and developmental capacity of human oocytes', Human Reproduction, 34, pp. 1-15.
- Vuong, L.N., Le, A.H., Ho, V.N.A., Pham, T.D., Sanchez, F., Leuzinger, L., Heindryckx, B., Smitz, J. and Mol, B.W. (2020) 'Effectiveness of biphasic in vitro maturation in women with polycystic ovary syndrome: a randomized controlled trial', Human Reproduction, 35(12), pp. 2737-2747.
연구 기록 날짜
연구 주요 날짜
연구 시작 (추정된)
기본 완료 (추정된)
연구 완료 (추정된)
연구 등록 날짜
최초 제출
QC 기준을 충족하는 최초 제출
처음 게시됨 (실제)
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
QC 기준을 충족하는 마지막 업데이트 제출
마지막으로 확인됨
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?
약물 및 장치 정보, 연구 문서
미국 FDA 규제 의약품 연구
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