- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT01033474
Results Following the Vitrification of Human Oocytes Using 2 Methodologies
Embryonic Developmental Rates and Pregnancies Following the Vitrification of Human Oocytes Using Two Methodologies.
The investigators are going to compare embryo developmental rates of human eggs following freezing in two different freezing methods. The investigators are going to compare the pregnancy rates following transfer to patients as well.
Null Hypothesis: The type of vitrification methodology used will not have an impact on the following:
- Survival rates
- Embryonic developmental rates
- Pregnancy and implantation rates.
Studieoversikt
Status
Forhold
Detaljert beskrivelse
Randomization of Oocytes: Oocytes will be denuded approximately 1-2 hours post retrieval and graded for maturity. Only the Metaphase II oocyte will be vitrified. Half of the oocytes within each donor will be randomized to the following treatments.
- Frozen using an open system using a metal grid to hold the oocyte. Three to five oocytes will be frozen on the metal grid using a minute amount (< 2-3 µls) of cryoprotectant. A top is put over the metal grid to protect the oocytes. This system has proven to be successful in limited cases in Peru. This is an open system of vitrification where the oocytes are directly plunged into liquid nitrogen. This will serve as the control.
- Frozen in closed straws using a methodology developed by Jim Stachecki. Three to five oocytes will be frozen in ¼ cc straws. This is very similar to the method used to successfully vitrify blastocysts. This will be the experimental treatment.
Null Hypothesis: The type of vitrification methodology used will not have an impact on the following:
- Survival rates
- Embryonic developmental rates
Pregnancy and implantation rates. Measured Outcomes The effect of vitrification technique will be measured using the appropriate statistical analysis on the following parameters.
- Survival rates following thawing.
- Effect of vitrification technique on how oocytes react to ICSI. The parameters have been previously defined at NCRS.
- Normal fertilization rates, abnormal fertilization rates and rates of degeneration following ICSI.
- Embryonic development rates. Embryos will be cultured until Day 5/6 and rate as well as quality of blastocyst will be noted.
- Pregnancy and implantation rates following replacement in endometrial prepared recipients.
Studietype
Registrering (Forventet)
Kontakter og plasseringer
Studiesteder
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Lima, Peru
- Laboratorio de Reproducción Asistida
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Deltakelseskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
Tar imot friske frivillige
Kjønn som er kvalifisert for studier
Prøvetakingsmetode
Studiepopulasjon
Beskrivelse
Inclusion Criteria:
- Must be healthy and pass testing as per clinic standards
Exclusion Criteria:
- Are over the age or cannot carry a pregnancy safely
Studieplan
Hvordan er studiet utformet?
Designdetaljer
Kohorter og intervensjoner
Gruppe / Kohort |
|---|
|
donor eggs
|
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infertile patients
|
Hva måler studien?
Sekundære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
Pregnancy rate
Tidsramme: 12 weeks
|
12 weeks
|
Samarbeidspartnere og etterforskere
Studierekorddatoer
Studer hoveddatoer
Studiestart
Primær fullføring (Forventet)
Studiet fullført (Faktiske)
Datoer for studieregistrering
Først innsendt
Først innsendt som oppfylte QC-kriteriene
Først lagt ut (Anslag)
Oppdateringer av studieposter
Sist oppdatering lagt ut (Anslag)
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Sist bekreftet
Mer informasjon
Begreper knyttet til denne studien
Nøkkelord
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- 555-2009
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