Clinical Trials Directory

Trials / Completed

CompletedNCT06555731

Ultra Rapid GEnome Sequencing

Long-read Human Genome Sequencing in 72 Hours: "Ultra Rapid GEnome Sequencing"

Status
Completed
Phase
Study type
Observational
Enrollment
4 (actual)
Sponsor
CMC Ambroise Paré · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

Next-generation sequencing (NGS) has revolutionized the field of genomics, allowing the detection of genetic abnormalities for diagnostic or therapeutic purposes. Turnaround times for exome or genome sequencing results have decreased to an average of 3 to 6 months. An increasing number of diagnostic and therapeutic fields are benefiting from the advancements in ultra-rapid sequencing. In some situations, a shorter turnaround time may be useful for making therapeutic and/or interventional management decisions. This study aims to explore the feasibility of very rapid whole-genome sequencing, ultra-rapid genome sequencing (URGES) in 72 hours, that could benefit patients with cancer or rare diseases.

Detailed description

* Blood sample (5 ml) * Extraction of genomic DNA from lymphocytes * Ultra-rapid genome sequencing (48 hours for a whole genome), using the PromethION P2 Solo sequencer (Oxford Nanopore Technologies) * Bioinformatics analysis of raw high-throughput sequencing data with SeqOne platform * Medical interpretation of molecular data: NGS data must be interpreted by a multidisciplinary decision-support team to determine mutation actionability and identify potential "drivers"

Conditions

Interventions

TypeNameDescription
GENETICUltra rapid genome sequencingDNA extraction from blood sample and whole genome sequencing

Timeline

Start date
2024-10-08
Primary completion
2024-10-12
Completion
2024-10-12
First posted
2024-08-15
Last updated
2024-12-18

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT06555731. Inclusion in this directory is not an endorsement.