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NCT03832634

Fetal Genome Profiling Via Trophoblast Cells

Terminated NA Last updated 3 August 2023
What this trial tests

NA trial testing Fetal Genome Profiling. in Fetal Growth Retardation in 1 participant. Terminated before completion.

Timeline
2 July 2020
Primary endpoint
14 February 2021
2 February 2023

Quick facts

Lead sponsorWeill Medical College of Cornell University
PhaseNA
StatusTerminated
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposediagnostic
Enrollment1
Start date2 July 2020
Primary completion14 February 2021
Estimated completion2 February 2023
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Weill Medical College of Cornell University

Who can join

Adults 18 to 45, female only, with Fetal Growth Retardation. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The objective of this study is to utilize trophoblast cells accumulating in the endocervical canal at the beginning of pregnancy for non-invasive prenatal testing. If we are able to validate that trophoblast cells obtained at an early gestational age can be reliably used for prenatal testing, there is great potential to improve early pregnancy management and counseling options for potential parents. The target population will be all women between the age of 18-45 undergoing care at the Center for Reproductive Medicine (CRM) in order to achieve a pregnancy.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Fetal Growth Retardation

Currently open trials in the same condition.

Other Weill Medical College of Cornell University trials

Trials by the same sponsor.

Verify against primary sources

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/NCT03832634.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing