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NCT04986657 · ClinicalTrials.gov registry record · NA

Whole Genome Sequencing (ChromoSeq) as an Adjunct to Conventional Genomic Profiling in AML and MDS

A NA study of Acute Myeloid Leukemia and Myelodysplastic Syndromes, sponsored by Washington University School of Medicine.

Recruiting
Registry status
NA
Development phase
325
Enrollment target
1
Study location

NCT04986657 is a NA study of Acute Myeloid Leukemia and Myelodysplastic Syndromes that is actively recruiting participants, run by Washington University School of Medicine. The registered enrollment target is 325 participants, above the 115-participant average among 306 other Acute Myeloid Leukemia trials with a reported enrollment target (183% higher). The trial reports 1 study location across 1 state.

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The verdict

NCT04986657, a NA study of Acute Myeloid Leukemia and Myelodysplastic Syndromes, is actively recruiting participants, sponsored by Washington University School of Medicine.

RECRUITING
Registry status
NA
Development phase
325 participants
Enrollment target
1
Study location

Study Summary

This is a single institution, prospective study of the whole genome sequencing assay, ChromoSeq. Using prospectively collected patient data, coupled with physician surveys, the investigators seek to determine the feasibility of implementing ChromoSeq in addition to standard genomic testing, for patients with the diagnoses of acute myeloid leukemia (AML) or myelodysplastic syndrome (MDS).

Interventions

  • DEVICE ChromoSeq

Study Locations (1)

Missouri

  • Washington University School of Medicine - St Louis

Trial Details

FieldValue
Enrollment Target 325 participants
Start Date 2021-09-17
Est. Completion 2027-12-31
Phase NA

What the Registry Record Tells You About NCT04986657

The ClinicalTrials.gov registry entry for NCT04986657 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 325 participants, a figure that helps gauge the scale of data the investigators plan to collect, above the 115-participant average among 306 other Acute Myeloid Leukemia trials with a reported enrollment target (183% higher). The listed sponsor is Washington University School of Medicine, which has 1,502 total studies on file at ClinicalTrials.gov.

The record links to 3 conditions, with Acute Myeloid Leukemia appearing as the primary indexed condition, and to 1 intervention - of which ChromoSeq is the first listed.

NCT04986657 reports 1 study location spanning 1 distinct geographic area - top geographies include Missouri.

Frequently Asked Questions

What is clinical trial NCT04986657 about?

NCT04986657 is a clinical study titled "Whole Genome Sequencing (ChromoSeq) as an Adjunct to Conventional Genomic Profiling in AML and MDS". This is a single institution, prospective study of the whole genome sequencing assay, ChromoSeq. Using prospectively collected patient data, coupled with physician surveys, the investigators seek to determine the feasibility of implementing ChromoSeq in addition to standard genomic testing, for pati...

What is the current status of trial NCT04986657?

This trial is currently recruiting. It is a NA study. The enrollment target is 325 participants. The study started on 2021-09-17. Estimated completion is 2027-12-31.

What conditions does trial NCT04986657 study?

This clinical trial studies the following conditions: Acute Myeloid Leukemia, Myelodysplastic Syndromes, Whole Genome Sequencing.

What interventions are being tested in trial NCT04986657?

The interventions under investigation include: ChromoSeq (DEVICE).

Who is sponsoring clinical trial NCT04986657?

This trial is sponsored by Washington University School of Medicine, which has 1,502 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT04986657 being conducted?

This trial has 1 study location across Missouri. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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