- ICH GCP
- Rejestr badań klinicznych w USA
- Badanie kliniczne NCT07429097
Pilotażowe badanie porzuconych blastocyst (DECODE)
Prospektywne, obserwacyjne badanie pilotażowe odrzuconych blastocyst: podejście molekularne do odkrywania ukrytego potencjału reprodukcyjnego
The goal of this observational study is to determine multiomics patterns related to global embryo quality to help overcome the limitations of conventional embryo quality assessment. The main question it aims to answer is:
• Do discarded blastocysts that reach the blastocyst stage (days 5-6) show characteristic multiomics profiles which correlate with chromosomal abnormalities, providing insights into embryo viability?
For that, patients undergoing an IVF treatment will be asked to donate their clinically discarded 5/6-day embryos (those that do not meet clinical criteria to be used for reproductive purposes). Participation in the study will not interfere with the planned IVF treatment. Patient participation is limited to signature of the informed consent to donate embryos and no other study-specific procedures will be performed on participants.
Przegląd badań
Status
Warunki
Interwencja / Leczenie
Szczegółowy opis
In vitro fertilization has advanced infertility treatment, but accurately assessing embryo viability remains challenging because conventional selection methods may miss subtle molecular indicators of developmental potential. Increasing evidence shows that some embryos discarded based on morphology or developmental timing may be chromosomally normal and possess favorable molecular traits, prompting interest in multiomics analysis as a more sensitive assessment tool. Studies have demonstrated that omics patterns can distinguish chromosomally normal from abnormal embryos and correlate with key indicators of developmental competence, such as morphology, arrest status, and implantation success, with high-potential blastocysts showing distinct developmental gene signatures. The blastocyst stage is particularly critical, as inner cell mass (ICM) and trophectoderm (TE) lineages diverge, and emerging data suggest these cell types exhibit different multiomics responses to chromosomal abnormalities. However, many prior studies relied on vitrified embryos, where cryopreservation may alter multiomic profiles.
To address this limitation, this study focuses on fresh, non-vitrified blastocysts, offering a more accurate representation of embryos' intrinsic molecular states and developmental potential. Therefore, the aim of the present pilot study is to define multiomics patterns associated with euploidy, chromosomal abnormalities and embryo quality at the blastocyst stage.
Once the study is approved by the competent Research Ethics Committee, the recruitment and selection of patients will follow. Every potential participant will be asked to sign the study informed consent. To comply with the study design and the proposed hypothesis, an estimated total number of 150 patients will be recruited to obtain around 200 discarded embryos.
This is a prospective, descriptive, observational pilot study which will include all eligible discarded blastocysts donated by IVF patients from a single Norwegian centre. This site will be responsible for patients' recruitment and embryonic samples collection, while sample analysis will take place in a Central Laboratory in Spain. On day 5/6 of development, blastocysts that do not meet the standard clinical criteria to be transferred, will be donated to the study by the participants. Additionally, when possible, cumulus cells and sperm cells will also be collected. After embryo donation, 2 trophectoderm and 1 inner cell mass biopsies will be collected and analysed for multiomics profiling.
Data exported from the medical records and source documents will be duly codified to protect the clinical and personal information of patients in accordance with the current legislation on data protection. This information will be exported to an internal database.
Participants' involvement in the study will be limited to the consent; participants will not undergo any other study specific procedures.
Typ studiów
Zapisy (Szacowany)
Kontakty i lokalizacje
Kontakt w sprawie studiów
- Nazwa: Carlos Gómez De La Cruz, PhD
- Numer telefonu: (+34) 963905310
- E-mail: carlos.gomez@vitrolifegroup.com
Kopia zapasowa kontaktu do badania
- Nazwa: Esperanza Irles Vidal, PhD
- E-mail: esperanza.irles@vitrolifegroup.com
Lokalizacje studiów
-
-
Oslo
-
Oslo, Oslo, Norwegia, 0372
- Rekrutacyjny
- Oslo University Hospital HF (OUS HF), Rikshospitalet
-
Kontakt:
- Maria Biba, PhD
- Numer telefonu: (+47) 94816156
- E-mail: marbib@ous-hf.no
-
Kontakt:
- Maria Vera, PhD
- E-mail: mavrod@ous-hf.no
-
Główny śledczy:
- Maria Biba, PhD
-
-
Kryteria uczestnictwa
Kryteria kwalifikacji
Wiek uprawniający do nauki
Akceptuje zdrowych ochotników
Płeć kwalifikująca się do nauki
Metoda próbkowania
Badana populacja
The study will involve 200 discarded embryos from approximately 150 women undergoing IVF treatment at Oslo University Hospital. The selected population will fall within the age range of 20 to 42, representing the common demographic for IVF patients.
Opis
Inclusion Criteria:
- Patients whose written informed consent approved by the Ethic Committee has been obtained, after having been duly informed of the nature of the study and voluntarily accepted to participate after being fully aware of the potential risks, benefits, and any discomfort involved.
- Patients undergoing regular IVF/ICSI cycles with fresh oocytes and embryo culture to the blastocyst stage (day 5-6 after fertilization)
- Patients' age will be between 20-42 years of age.
- Patients without PGT-M or PGT-SR indication.
Exclusion Criteria:
- Patients who do not have at least one discarded blastocyst on day 5-6 of development.
- Patients with discarded blastocysts that do not meet these criteria:
- Presence of ICM
- Non-degenerated
Plan studiów
Jak projektuje się badanie?
Szczegóły projektu
- Modele obserwacyjne: OTHER
- Perspektywy czasowe: PROSPECTIVE
Kohorty i interwencje
Grupa / Kohorta |
Interwencja / Leczenie |
|---|---|
|
Discarded blastocysts
All study participants will follow the same procedure. Study participation is limited to informed consent signature and donation of the clinically discarded embryos. Participants will not undergo any other study-specific procedures. |
Donated discarded blastocysts (day 5/6) will undergo 2 TE biopsies and 1 ICM biopsy which will be analyzed for chromosomic status and multiomics profiles. Additional, when possible, cumulus cells and sper cells will also be analyzed. After donation of the discarded embryos, participants will follow their established IVF treatment. |
Co mierzy badanie?
Podstawowe miary wyniku
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
|
Establishment of multiomics patterns associated with euploidy, chromosomal abnormalities and embryo quality at the blastocyst stage.
Ramy czasowe: 1 day, corresponding to the Informed Consent signature date.
|
Discarded embryos will be analyzed for multiomics and bioinformatic analysis will be applied to find multiomics patterns that correlate with euploidy, chromosomal abnormalities and embryo quality. |
1 day, corresponding to the Informed Consent signature date.
|
Miary wyników drugorzędnych
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
|
Determination of the genetic constitution of different blastocyst compartments.
Ramy czasowe: 1 day, corresponding to the Informed Consent signature date.
|
Comparison of the genetic constitution of trophectoderm (TE) and inner cell mass (ICM) biopsies from the same blastocyst. |
1 day, corresponding to the Informed Consent signature date.
|
|
Determination of the incidence of chromosomally normal blastocysts with normal fertilization (2PN) that have been discarded due to poor morphology, slow development or cell degeneration.
Ramy czasowe: 1 day, corresponding to the Informed Consent signature date.
|
Chromosomic dotation of 2PN blastocysts that have been discarded (due to poor morphology, slow development or cell degeneration) will be analyzed for chromosomal status and the ratio of normal blastocysts will be calculated. |
1 day, corresponding to the Informed Consent signature date.
|
|
Determination of the incidence of chromosomally normal blastocysts in blastocysts with atypical fertilization (0PN, 1PN, 3PN).
Ramy czasowe: 1 day, corresponding to the Informed Consent signature date.
|
Chromosomic dotation of atypically fertilized blastocysts (0PN, 1PN, 2PN) will be analyzed and the ratio of chromosomically normal blastocysts will be calculated. |
1 day, corresponding to the Informed Consent signature date.
|
|
Exploration of the potential contamination of TE biopsies with cumulus and sperm cells and its possible impact on the accuracy of the results.
Ramy czasowe: 1 day, corresponding to the Informed Consent signature date.
|
Genetic analysis of the TE biopsies will be compared with the genetic analysis of cumulus cells and sperm cells for possible DNA contamination in the TE biopsy. |
1 day, corresponding to the Informed Consent signature date.
|
|
Correlation of embryo morphokinetics parameters with the TE and ICM chromosomal status.
Ramy czasowe: 1 day, corresponding to the Informed Consent signature date.
|
Genetic analysis of the TE and ICM biopsies will be compared with embryo morphokinetics parameters to find any correlations. |
1 day, corresponding to the Informed Consent signature date.
|
|
Correlation of embryo morphokinetics parameters with the TE and ICM multiomics profiles.
Ramy czasowe: 1 day, corresponding to the Informed Consent signature date.
|
Multiomics profiling of the TE and ICM biopsies will be compared with embryo morphokinetics parameters to find any correlations. |
1 day, corresponding to the Informed Consent signature date.
|
|
Correlation of sibling relatedness with multiomics profiles in cases with more than one embryo available per cycle
Ramy czasowe: 1 day, corresponding to the Informed Consent signature date.
|
When more than one embryo is discarded from the same cycle, they will be analysed to find a possible correlation between sibling relatedness and multiomics profiles. |
1 day, corresponding to the Informed Consent signature date.
|
Współpracownicy i badacze
Sponsor
Współpracownicy
Śledczy
- Krzesło do nauki: Carmen Rubio, PhD, Vicepresident R&D Genetic Services
Daty zapisu na studia
Główne daty studiów
Rozpoczęcie studiów (Rzeczywisty)
Zakończenie podstawowe (Szacowany)
Ukończenie studiów (Szacowany)
Daty rejestracji na studia
Pierwszy przesłany
Pierwszy przesłany, który spełnia kryteria kontroli jakości
Pierwszy wysłany (Rzeczywisty)
Aktualizacje rekordów badań
Ostatnia wysłana aktualizacja (Rzeczywisty)
Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości
Ostatnia weryfikacja
Więcej informacji
Terminy związane z tym badaniem
Słowa kluczowe
Dodatkowe istotne warunki MeSH
Inne numery identyfikacyjne badania
- IGX-DEC-CR-25-03
Plan dla danych uczestnika indywidualnego (IPD)
Planujesz udostępniać dane poszczególnych uczestników (IPD)?
Informacje o lekach i urządzeniach, dokumenty badawcze
Bada produkt leczniczy regulowany przez amerykańską FDA
Bada produkt urządzenia regulowany przez amerykańską FDA
Te informacje zostały pobrane bezpośrednio ze strony internetowej clinicaltrials.gov bez żadnych zmian. Jeśli chcesz zmienić, usunąć lub zaktualizować dane swojego badania, skontaktuj się z register@clinicaltrials.gov. Gdy tylko zmiana zostanie wprowadzona na stronie clinicaltrials.gov, zostanie ona automatycznie zaktualizowana również na naszej stronie internetowej .