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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT01780415
Other study ID # NewEra21972
Secondary ID
Status Active, not recruiting
Phase
First received
Last updated
Start date January 2013
Est. completion date January 2022

Study information

Verified date February 2021
Source Cervesi Hospital, Cattolica, Italy
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The objective will focus on the characterization of DNA fragments present in Blastocoele fluid, and the evaluation of these fragments as potential target for Preimplantation Genetic Diagnosis. To reach this goal, real-time PCR, Whole Genome Amplification techniques and -subsequently- Next Generation Sequencing and aCGH approaches will be used.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 35
Est. completion date January 2022
Est. primary completion date December 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 40 Years
Eligibility Inclusion Criteria: - IVF patient with supernumerary embryos to vitrify at blastocyst stage Exclusion Criteria: - IVF patient without blastocyst formation

Study Design


Related Conditions & MeSH terms


Intervention

Other:
blastocoele aspiration


Locations

Country Name City State
Italy Cervesi Hospital IVF Unit Cattolica Rimini

Sponsors (1)

Lead Sponsor Collaborator
Cervesi Hospital, Cattolica, Italy

Country where clinical trial is conducted

Italy, 

Outcome

Type Measure Description Time frame Safety issue
Primary Number of samples with DNA in blastocoele Fluid the presence of DNA will be evaluated through rtPCR 6 month
Secondary Number of euploid samples Array CGH 8 months