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NCT03622892: NID

Non-invasive Prenatal Diagnosis of Monogenic Disorders by Linked-reads Technology

Status unknown Last updated 27 January 2020
What this trial tests

trial in Cystic Fibrosis in 75 participants. Status unknown.

Timeline
18 October 2018
Primary endpoint
18 October 2021
18 October 2021

Quick facts

Lead sponsorUniversity Hospital, Brest
StatusStatus unknown
Study typeOBSERVATIONAL
Enrollment75
Start date18 October 2018
Primary completion18 October 2021
Estimated completion18 October 2021
Sites6 locations across France

Conditions studied

Sponsor

University Hospital, Brest

Who can join

Adults 18 to 55, any sex, with Cystic Fibrosis. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Description of the presence of cell-free fetal DNA in maternal plasma allowed the possibility of non-invasive prenatal diagnosis. Whereas detection of paternally-inherited alleles is straightforward and being quickly implemented in routine, detection of maternally-inherited alleles remains challenging. To date, the main approach that is being developped, called Relative Haplotype Dosage Analysis, relies on the identification of an allelic imbalance between the mother's wild-type and mutant alleles, relative to the fetal's contribution. This approach therefore requires the study of a propositus to identify the morbid haplotype, which is not always possible in the context of an ongoing pregnancy. In this study, we aim to evaluate the contribution of new technologies, such as linked-read Sequencing, to allow direct identification of parental haplotype in the context of non-invasive prenatal diagnosis.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Cystic Fibrosis

Currently open trials in the same condition.

Other University Hospital, Brest 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/NCT03622892.

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