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NCT05936749

Pre-implantation Genetic Testing for Monogenic Disease: Single Center Experience

Completed Last updated 10 July 2023
What this trial tests

trial testing Pre-implantation genetic testing in Genetic Disease in 76 participants. Completed in 12 December 2022.

Timeline
2 January 2016
Primary endpoint
12 December 2022
12 December 2022

Quick facts

Lead sponsorIstituto Clinico Humanitas
StatusCompleted
Study typeOBSERVATIONAL
Enrollment76
Start date2 January 2016
Primary completion12 December 2022
Estimated completion12 December 2022

Drugs / interventions tested

Conditions studied

Sponsor

Istituto Clinico Humanitas

Who can join

Adults 34 to 42, female only, with Genetic Disease or Aneuploidy. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This monocentric retrospective observational study aims to evaluate the efficacy of pre-implantation genetic testing for monogenic diseases (PGT-M). The effectiveness will be assessed in terms of live birth rate (LBR), cumulative live birth rate (CLBR) per couple, and abortion rate (AR). Considering how many cycles the participants have undergone to achieve a viable blastocyst. The secondary objective is to evaluate the incidence of aneuploidy in unaffected embryos, in order to understand the need for pre-implantation genetic testing for aneuploidy (PGT-A)in addition to PGT-M.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other recruiting trials for Genetic Disease

Currently open trials in the same condition.

Other Istituto Clinico Humanitas trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05936749.

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