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HELIOS Advanced: Human Embryo Illumination to Enhance Development (HELIOS-A)

5 de novembro de 2026 atualizado por: Samuel Zev Williams, Columbia University

HELIOS Advanced: Iluminação de Oócitos Humanos para Melhorar o Desenvolvimento

As women get older, the "power plants" of the cells (called mitochondria) don't work as well. This makes it harder for eggs and embryos to develop normally. One possible way to help is with a gentle light treatment called photobiomodulation (PBM). This uses a special type of red light that boosts energy production in cells and helps them stay healthy. This study will test whether adding this light treatment during in vitro fertilization (IVF) can improve embryo growth and pregnancy outcomes.

Visão geral do estudo

Status

Recrutamento

Intervenção / Tratamento

Descrição detalhada

Embryo development is highly energy-dependent, and impaired mitochondrial function is a well-established hallmark of reproductive aging. As women age, reactive oxygen species (ROS) accumulate and cause mitochondrial DNA (mtDNA) damage, leading to reduced oxidative phosphorylation, ATP (Adenosine 5'-triphosphate) depletion, and developmental arrest of embryos. Enhancing mitochondrial function represents a promising strategy to improve embryo quality, particularly in women of advanced maternal age.

Photobiomodulation (PBM), also known as low-level light therapy (LLLT), involves the application of low-intensity red or near-infrared (NIR) light to modulate mitochondrial activity. NIR light specifically activates cytochrome c oxidase, leading to increased ATP production, reduced oxidative stress, and improved cellular resilience. Numerous preclinical studies, including isolated mitochondria, cell cultures, and in vivo animal models, have confirmed the safety and efficacy of NIR light in restoring mitochondrial function without inducing DNA damage or chromosomal abnormalities.

The investigators previously conducted IRB-approved laboratory studies using mouse and donated human embryos, demonstrating that brief exposure to PBM improved blastocyst formation without adversely affecting chromosomal status.

The current study builds upon this foundational work to evaluate the clinical impact of PBM at the oocyte stage. In a randomized, blinded, sibling-embryo design, the investigators will test whether PBM improves fertilization rates, blastocyst formation, embryo quality, and pregnancy outcomes in participants undergoing IVF or ICSI (Intracytoplasmic sperm injection) with PGT-A (preimplantation genetic testing for aneuploidy) using their autologous oocytes.

Tipo de estudo

Intervencional

Inscrição (Estimado)

270

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.

Contato de estudo

Locais de estudo

    • New York
      • New York, New York, Estados Unidos, 10019
        • Recrutamento
        • Columbia University Fertility Center
        • Investigador principal:
          • Samuel Z Williams, MD, PhD
        • Contato:

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

18 anos a 48 anos (Adulto)

Aceita Voluntários Saudáveis

Sim

Gêneros Elegíveis para o Estudo

Fêmea

Descrição

Inclusion Criteria:

  • Female age between 18-48 years at the time of the IVF/ICSI cycle
  • Undergoing blastocyst culture
  • Using own oocytes
  • Has at least two cleavage stage embryos available for randomization on Day 3 of embryo development
  • Consenting to embryo level randomization
  • Plan to transfer euploid embryo within 6 months

Exclusion Criteria:

  • Use of donor oocytes or gestational carrier
  • Concurrent experimental laboratory inventions outside of protocol
  • Refusal of randomization or request for non-standard handling

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: Triplo

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Sem intervenção: No photobiomodulation

Participants will receive the same treatment (IVF/ICSI cycles with PGT-A). Participant's resultant cleavage stage embryos will be randomized to not receive PBM.

Experimental: Photobiomodulation

Participants will receive the same treatment (IVF/ICSI cycles with PGT-A). Participant's resultant cleavage stage embryos will be randomized to receive PBM.

Photobiomodulation (PBM): also known as low-level light therapy (LLLT), involves the application of low-intensity red or near-infrared (NIR) light to modulate mitochondrial activity.

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Number of usable blastocysts
Prazo: Seven days post egg retrieval

Usable blastocysts are defined as blastocysts that can be biopsied and frozen on Day 5, 6, or 7 of development for PGT-A (pre-implantation genetic testing for aneuploidy). The study will calculate the usable blastocyst rate per oocyte retrieved defined as the number of usable blastocysts per cleavage stage embryo on Day 3.

Seven days post egg retrieval

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
Time to 2-cell stage
Prazo: Up to seven days post egg retrieval

Time (hours) for embryo to reach the 2-cell stage from insemination/ICSI as assessed by embryology using time-lapse imaging.

Up to seven days post egg retrieval
Time to 3-cell stage
Prazo: Up to seven days post egg retrieval

Time (hours) for embryo to reach the 3-cell stage from insemination/ICSI as assessed by embryology using time-lapse imaging.

Up to seven days post egg retrieval
Time to 6-cell stage
Prazo: Up to seven days post egg retrieval

Time (hours) for embryo to reach the 6-cell stage from insemination/ICSI as assessed by embryology using time-lapse imaging.

Up to seven days post egg retrieval
Time to 8-cell stage
Prazo: Up to seven days post egg retrieval

Time (hours) for embryo to reach the 8-cell stage from insemination/ICSI as assessed by embryology using time-lapse imaging.

Up to seven days post egg retrieval
Time to morula
Prazo: Up to seven days post egg retrieval

Time (hours) for embryo to reach the morula stage from insemination/ICSI as assessed by embryology using time-lapse imaging.

Up to seven days post egg retrieval
Time to start of blastulation
Prazo: Up to seven days post egg retrieval

Time (hours) for embryo to start blastulation from insemination/ICSI as assessed by embryology using time-lapse imaging.

Up to seven days post egg retrieval
Time to blastocyst
Prazo: Up to seven days post egg retrieval

Time (hours) for embryo to reach the blastocyst stage from insemination/ICSI as assessed by embryology using time-lapse imaging.

Up to seven days post egg retrieval
Time to hatching blastocyst
Prazo: Up to seven days post egg retrieval

Time (hours) for embryo to reach the hatching blastocyst stage from insemination/ICSI as assessed by embryology using time-lapse imaging.

Up to seven days post egg retrieval
Number of good quality blastocysts as defined by Gardner grading system
Prazo: Up to seven days post egg retrieval

Final blastocyst quality at the time of cryopreservation (Day 5,6, or 7) will be assessed using the Gardner grading system, which consists of three parameters: expansion and hatching status (graded 1-6), inner cell mass (graded A-D), and trophectoderm (graded A-D). A good quality blastocyst will be defined as a blastocyst of grade 3BB or higher.

Up to seven days post egg retrieval
Euploidy Rate
Prazo: Within 30 days post egg retrieval

The chromosomal ploidy status of cryopreserved blastocysts is assessed by the presence of two copies of each autosome and the expected complement of sex chromosomes. The euploidy rate is defined as the number of cryopreserved blastocysts that have the correct number of chromosomes divided by the total number of cryopreserved blastocysts.

Within 30 days post egg retrieval
Proportion of Embryo Selected for Transfer
Prazo: Within 1 year post egg retrieval

In cases with no stated embryo sex preference, the proportion of cycles in which the embryo selected for transfer is from the PBM-treated group versus the control group will be reported.

Within 1 year post egg retrieval
Implantation Rate
Prazo: Within 1 year post egg retrieval

Implantation rate is defined as the number of cycles with positive beta hCG (human chorionic gonadotropin) nine days or more post frozen embryo transfer divided by the total number of frozen embryo transfer cycles.

Within 1 year post egg retrieval
Clinical pregnancy rate
Prazo: Within 1 year post egg retrieval

Clinical pregnancy rate is defined as the number of cycles with the presence of a gestational sac visualized on transvaginal ultrasound divided by the total number of frozen embryo transfer cycles.

Within 1 year post egg retrieval
Miscarriage rate
Prazo: Within 1 year of egg retrieval

Miscarriage rate is defined as the number of cycles with clinical pregnancy losses divided by the number of cycles that had positive hCGs post frozen embryo transfer.

Within 1 year of egg retrieval
Live birth rate
Prazo: Up to 2 years post egg retrieval

Live birth rate is defined as the number of cycles with a live born infant after 24 weeks gestation divided by total number of frozen embryo transfer cycles.

Up to 2 years post egg retrieval
Gestational Age at Delivery
Prazo: Up to 2 years post egg retrieval

Total number of completed weeks and days of pregnancy, calculated using frozen embryo transfer date.

Up to 2 years post egg retrieval
Birthweight
Prazo: Up to 2 years post egg retrieval

The weight of the baby at birth in grams

Up to 2 years post egg retrieval

Colaboradores e Investigadores

É aqui que você encontrará pessoas e organizações envolvidas com este estudo.

Patrocinador

Investigadores

  • Investigador principal: Samuel Zev Williams, MD/PhD, Columbia University

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)

24 de março de 2026

Conclusão Primária (Estimado)

1 de junho de 2027

Conclusão do estudo (Estimado)

1 de junho de 2028

Datas de inscrição no estudo

Enviado pela primeira vez

13 de fevereiro de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

13 de fevereiro de 2026

Primeira postagem (Real)

20 de fevereiro de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

9 de novembro de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

5 de novembro de 2026

Última verificação

1 de novembro de 2026

Mais Informações

Termos relacionados a este estudo

Outros números de identificação do estudo

  • ACYY1279

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