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- Registro de ensaios clínicos dos EUA
- Ensaio Clínico NCT07771283
Purpose to Evaluate the Effectiveness of the Superovulation Stimulation Protocol Using Human Chorionic Gonadotropin (hCG) by Demonstrating Its Equivalence to Standard Controlled Ovarian Stimulation Protocols in Terms of Oocytes Retrieved, Blastulation While Maintaining an Economic Advantage
26 de agosto de 2026 atualizado por: Oleksandr Plyh, LTD "EKODNIPRO", Medical centre Medical Plaza Dnipro
Prospective Randomized Single-Blind Study of the Effectiveness of the Superovulation Stimulation Protocol Using hCG Compared to Standard Protocols With Different Gonadotropin Doses in In Vitro Fertilization Programs
This study evaluates a more affordable medication protocol for ovarian stimulation during in vitro fertilization (IVF).
Standard IVF protocols use medications called gonadotropins to stimulate the ovaries to produce multiple eggs, but these medications can be very expensive and create a barrier to treatment.
This clinical trial tests whether substituting a significant portion of these standard medications with human chorionic gonadotropin (hCG) is just as effective.
Researchers will compare the number and quality of eggs and embryos produced by women using the experimental hCG protocol versus those using the standard gonadotropin protocol.
The main goal is to determine if the hCG method can provide similar clinical outcomes and safety profiles while significantly reducing the overall financial cost of IVF treatment.
Visão geral do estudo
Status
Inscrevendo-se por convite
Condições
- Infertilidade
- Mulheres inférteis submetidas a fertilização in vitro ou ICSI
- Simulação de ovário controlado
- Medicamentos para infertilidade
- Infertilidade (pacientes de fertilização in vitro)
- Mulheres inférteis submetidas à tecnologia de reprodução assistida (ART)
- Estimulação no ovário
- Tecnologia de Reprodução Assistida para Infertilidade
- Pacientes inférteis
- Infertile Women Undergoing ART
Descrição detalhada
Ovarian stimulation is a critical phase in assisted reproductive technologies (ART), but the high cost of recombinant gonadotropins remains a significant barrier to the accessibility of care for many patients.
Human chorionic gonadotropin (hCG), due to its structural similarity to luteinizing hormone (LH), binds to LH/hCG receptors and can effectively support steroidogenesis and folliculogenesis when administered in sub-trigger doses.
This prospective, randomized, single-blind trial is designed as a non-inferiority study to demonstrate that an hCG-based stimulation protocol is equivalent to standard controlled ovarian stimulation.
While standard protocols rely on the continuous administration of follicle-stimulating hormone (FSH) or FSH/LH, the experimental protocol introduces 200 IU of hCG (without FSH) to replace standard gonadotropins once the main cohort of follicles reaches 11 to 12 millimeters in size.
Both treatment arms will utilize a fixed gonadotropin-releasing hormone (GnRH) antagonist protocol starting on day 6 of stimulation, followed by a dual trigger for final oocyte maturation.
To minimize bias and ensure objective results, the embryologists evaluating oocyte morphology, fertilization rates, and blastocyst development will be blinded to the treatment arm assignments.
If moderate or severe ovarian hyperstimulation syndrome (OHSS) is suspected in the experimental group, the protocol incorporates safety measures, including switching to a GnRH agonist trigger and utilizing a "freeze-all" strategy.
By thoroughly comparing these methods through both intention-to-treat (ITT) and per-protocol (PP) analyses, researchers aim to validate an individualized treatment approach.
Proving the non-inferiority of this alternative protocol could potentially reduce the medication cost of an IVF cycle by 30 to 60 percent, providing clinicians with a flexible, cost-effective tool without compromising clinical efficacy or patient safety.
Tipo de estudo
Intervencional
Inscrição (Estimado)
360
Estágio
- Não aplicável
Contactos e Locais
Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.
Critérios de participação
Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.
Critérios de elegibilidade
Idades elegíveis para estudo
- Adulto
Aceita Voluntários Saudáveis
Não
Descrição
Inclusion Criteria:
- Women of reproductive age between 18 and 40 years.
- Clinical indications for the induction of superovulation (undergoing ART/IVF programs).
- Patients with all variants of ovarian reserve.
- Body Mass Index (BMI) up to 35 kg/m².
- Provision of informed consent to participate in the research study.
Exclusion Criteria:
- Presence of ovarian endometriomas.
- History of severe Ovarian Hyperstimulation Syndrome (OHSS) in previous cycles.
- Presence of severe endocrine disorders.
- History or presence of oncological diseases.
- Any medical contraindications to hormonal stimulation.
- Severe male factor infertility (specifically cryptozoospermia)
Plano de estudo
Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.
Como o estudo é projetado?
Detalhes do projeto
- Finalidade Principal: Tratamento
- Alocação: Randomizado
- Modelo Intervencional: Atribuição Paralela
- Mascaramento: Solteiro
Armas e Intervenções
Grupo de Participantes / Braço |
Intervenção / Tratamento |
|---|---|
|
Experimental: hCG Protocol
atients in this group undergo ovarian stimulation where human chorionic gonadotropin (hCG) replaces standard gonadotropins (or a significant portion of them) once the main cohort of follicles reaches 11-12 mm in size.
This arm utilizes a fixed gonadotropin-releasing hormone (GnRH) antagonist protocol starting on day 6 of stimulation and a dual trigger for final maturation.
|
Administered in sub-trigger doses of 200 IU (without FSH) as a substitute for LH activity and to support folliculogenesis
Administered starting on the 6th day of stimulation as part of a fixed antagonist protocol
Administered to induce final oocyte maturation before retrieval
Outros nomes:
Standard follicle-stimulating hormone (FSH) or FSH/LH preparations administered continuously at doses ranging from 100 to 225 IU/day.
Standard follicle-stimulating hormone (FSH) or FSH/LH preparations administered continuously at doses ranging from 100 to 225 IU/day before main cohort of follicles reach size 11-12mm
|
|
Comparador Ativo: Standard Protocol
Patients in this group undergo standard controlled ovarian stimulation using continuous administration of gonadotropins.
This arm also utilizes a fixed gonadotropin-releasing hormone (GnRH) antagonist protocol starting on day 6 of stimulation and a dual trigger for final maturation
|
Administered starting on the 6th day of stimulation as part of a fixed antagonist protocol
Administered to induce final oocyte maturation before retrieval
Outros nomes:
Standard follicle-stimulating hormone (FSH) or FSH/LH preparations administered continuously at doses ranging from 100 to 225 IU/day.
Standard follicle-stimulating hormone (FSH) or FSH/LH preparations administered continuously at doses ranging from 100 to 225 IU/day before main cohort of follicles reach size 11-12mm
|
O que o estudo está medindo?
Medidas de resultados primários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
Number of oocytes retrieved (oocyte yield)
Prazo: Day of oocyte retrieval (typically 34-36 hours after trigger administration)
|
The total count of oocytes retrieved following the controlled ovarian stimulation protocol
|
Day of oocyte retrieval (typically 34-36 hours after trigger administration)
|
|
Proportion of Mature Oocytes (MII Rate)
Prazo: Day of oocyte retrieval
|
Description: The percentage of retrieved oocytes that have reached the Metaphase II (MII) stage, evaluated according to the standardized ESHRE/ALPHA (Istanbul Consensus, 2025 update) criteria
|
Day of oocyte retrieval
|
|
Fertilization Rate
Prazo: Day 1 following oocyte retrieval
|
The percentage of mature oocytes (MII) that are successfully fertilized.
|
Day 1 following oocyte retrieval
|
|
Embryo Quality
Prazo: Day 3 and Day 5 following oocyte retrieval
|
The percentage of good quality cleavage-stage embryos and good quality blastocysts, assessed according to the standardized ESHRE/ALPHA (Istanbul Consensus, 2025 update) criteria.
|
Day 3 and Day 5 following oocyte retrieval
|
|
Total Dose of Gonadotropins/hCG
Prazo: From Day 1 of stimulation up to the day of trigger administration (approximately 10-14 days)
|
The total cumulative dose in International Units (IU) of gonadotropins or hCG administered throughout the entire stimulation cycle
|
From Day 1 of stimulation up to the day of trigger administration (approximately 10-14 days)
|
Medidas de resultados secundários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
Clinical Pregnancy Rate
Prazo: Approximately 4 to 6 weeks following embryo transfer
|
The percentage of patients who achieve a clinical pregnancy following embryo transfer
|
Approximately 4 to 6 weeks following embryo transfer
|
|
Live Birth Rate
Prazo: Approximately 9 to 10 months following embryo transfer
|
The percentage of patients who achieve a live birth
|
Approximately 9 to 10 months following embryo transfer
|
|
Incidence of Ovarian Hyperstimulation Syndrome (OHSS)
Prazo: From the day of trigger administration through the luteal phase/early pregnancy
|
The frequency of moderate and severe OHSS cases, classified according to RCOG/ESHRE criteria
|
From the day of trigger administration through the luteal phase/early pregnancy
|
|
Average Duration of Stimulation
Prazo: From Day 1 of stimulation up to the day of trigger administration (approximately 10-14 days)
|
The total number of days the stimulation medications were administered.
|
From Day 1 of stimulation up to the day of trigger administration (approximately 10-14 days)
|
|
Endometrial Thickness
Prazo: On the day of trigger administration
|
The thickness of the endometrium measured in millimeters (mm) via ultrasound
|
On the day of trigger administration
|
|
Cost of Stimulation Protocol per Cycle
Prazo: At the completion of the stimulation protocol (day of trigger)
|
An economic evaluation calculating the total cost of all medications consumed during the stimulation cycle, initially recorded in UAH and converted to USD.
|
At the completion of the stimulation protocol (day of trigger)
|
Colaboradores e Investigadores
É aqui que você encontrará pessoas e organizações envolvidas com este estudo.
Patrocinador
Colaboradores
Investigadores
- Investigador principal: Oleksandr O. Plyh, MD, LTD "EKODNIPRO"
Publicações e links úteis
A pessoa responsável por inserir informações sobre o estudo fornece voluntariamente essas publicações. Estes podem ser sobre qualquer coisa relacionada ao estudo.
Publicações Gerais
- Filicori M, Cognigni GE, Gamberini E, Parmegiani L, Troilo E, Roset B. Efficacy of low-dose human chorionic gonadotropin alone to complete controlled ovarian stimulation. Fertil Steril. 2005 Aug;84(2):394-401. doi: 10.1016/j.fertnstert.2005.02.036.
- Huong NTL, Thuy TT, Anh PTT, Long HB, Thang LD, Ngoc VT, Do LQ, Duy NXA, Hanh BT, Loi DV, Hoang L. Effects of 100 IU versus 150 IU hCG supplementation on oocyte and embryo quality in patients aged >/= 35 years: a propensity score-matched analysis. Int J Med Sci. 2025 Jan 27;22(4):982-989. doi: 10.7150/ijms.106965. eCollection 2025.
- Blockeel C, De Vos M, Verpoest W, Stoop D, Haentjens P, Devroey P. Can 200 IU of hCG replace recombinant FSH in the late follicular phase in a GnRH-antagonist cycle? A pilot study. Hum Reprod. 2009 Nov;24(11):2910-6. doi: 10.1093/humrep/dep253. Epub 2009 Jul 17.
- Lin H, Huang X, Zhao Y, Wang Y, Wang S, Hong F, Pan M, Liu L. Low-dose human chorionic gonadotropin supplementation initiated at the onset of ovarian stimulation can improve oocyte quality without impairing endometrial receptivity: Case series. Medicine (Baltimore). 2022 Dec 2;101(48):e32175. doi: 10.1097/MD.0000000000032175.
Datas de registro do estudo
Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.
Datas Principais do Estudo
Início do estudo (Real)
17 de agosto de 2026
Conclusão Primária (Estimado)
1 de fevereiro de 2028
Conclusão do estudo (Estimado)
1 de maio de 2028
Datas de inscrição no estudo
Enviado pela primeira vez
10 de agosto de 2026
Enviado pela primeira vez que atendeu aos critérios de CQ
14 de agosto de 2026
Primeira postagem (Real)
18 de agosto de 2026
Atualizações de registro de estudo
Última Atualização Postada (Real)
27 de agosto de 2026
Última atualização enviada que atendeu aos critérios de controle de qualidade
26 de agosto de 2026
Última verificação
1 de agosto de 2026
Mais Informações
Termos relacionados a este estudo
Palavras-chave
Termos MeSH relevantes adicionais
- Doenças urogenitais
- Doenças Genitais
- Doenças Urogenitais Femininas
- Doenças urogenitais femininas e complicações na gravidez
- Doenças Genitais Femininas
- Infertilidade
- Infertilidade Feminina
- Hormônios
- Hormônios, substitutos hormonais e antagonistas hormonais
- Hormônios que liberam hormônios da hipófise
- Hormônios hipotalâmicos
- Hormônios peptídicos
- Neuropeptídeos
- Peptídeos
- Aminoácidos, peptídeos e proteínas
- Oligopeptídeos
- Proteínas do tecido nervoso
- Proteínas
- Hormônios placentários
- Proteínas de gravidez
- Gonadotrofina Coriônica
- Hormônio liberador de gonadotrofina
- LHRH, AC-NAL (1) -CPA (2) -TRP (3) -Arg (6) -ALA (10)-
- Gonadotropins
Outros números de identificação do estudo
- 2 (Instituto Cardiovascular de Buenos Aires)
Plano para dados de participantes individuais (IPD)
Planeja compartilhar dados de participantes individuais (IPD)?
SIM
Descrição do plano IPD
De-identified individual participant data (IPD) that underlie the results reported in the final published article will be shared.
This includes data collected for the primary and secondary endpoints, after appropriate anonymization to ensure strict compliance with GDPR and Ukrainian data protection laws.
Prazo de Compartilhamento de IPD
Data will become available beginning 6 months and ending 36 months following article publication.
Critérios de acesso de compartilhamento IPD
Data will be shared with researchers who provide a methodologically sound proposal to achieve aims outlined in the approved proposal.
Proposals should be directed to the Principal Investigator.
To gain access, data requestors will need to sign a formal data access agreement.
Tipo de informação de suporte de compartilhamento de IPD
- PROTOCOLO DE ESTUDO
- CIF
Informações sobre medicamentos e dispositivos, documentos de estudo
Estuda um medicamento regulamentado pela FDA dos EUA
Não
Estuda um produto de dispositivo regulamentado pela FDA dos EUA
Não
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