Actively Recruiting

Early Phase 1
Age: 5Years +
All Genders
NCT07066085

Serial Blood Count Study

Led by University of Washington · Updated on 2025-07-15

20

Participants Needed

1

Research Sites

58 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The objective of the Serial Blood Count Study is to determine the utility of home monitoring of white blood cell (WBC) and absolute neutrophil counts (ANC) to diagnose cyclic neutropenia and distinguish between cyclic and severe congenital neutropenia (SCN). A new home monitoring device called Athelas One was granted an FDA 510K Class 2 clearance for evaluation of white blood count (WBC) and absolute neutrophil count (ANC). The investigators believe this device provides a unique and extremely valuable opportunity to for diagnosis of these diseases.

CONDITIONS

Official Title

Serial Blood Count Study

Who Can Participate

Age: 5Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Confirmed diagnosis of severe chronic neutropenia
  • 5 years of age or older, male or female
  • Known positive ELANE mutation
  • Computer if available
  • Internet access
  • Cell phone / Smart phone that can download / install applications (App)
  • Adults comfortable obtaining blood samples without medical conditions that complicate sample collection
Not Eligible

You will not qualify if you...

  • Diagnosis of severe chronic neutropenia with negative ELANE mutation results
  • Younger than 5 years of age
  • No internet access
  • No cell phone or smartphone capable of downloading/installing applications
  • Adults uncomfortable obtaining blood samples or with medical conditions that make sample collection difficult

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University of Washington Medical Center - Montlake

Seattle, Washington, United States, 98195

Actively Recruiting

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Research Team

A

Audrey Anna Bolyard, RN, BSN

CONTACT

D

David C. Dale, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

DIAGNOSTIC

Number of Arms

1

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