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Not yet recruiting Not applicable Interventional

Rethinking Early Airway Clearence Therapies

ClinicalTrials.gov ID: NCT07696338

Public ClinicalTrials.gov record NCT07696338. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 4, 2026, 4:34 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The REACT trial consists of two parallel, randomized studies; the Hypertonic Saline Study and the Dornase Alfa Study. Health outcomes among people with cystic fibrosis (CF) have been steadily improving, most recently with the advent of highly effective modulator therapy (HEMT). While therapies like hypertonic saline (HS) and dornase alfa (DA) improved outcomes in the past, they are often burdensome. Now that almost 90% of the North American CF population is being treated with elexacaftor/tezacaftor/ivacaftor (ETI) or vanzacaftor/tezacaftor/deutivacaftor (VTD), this trial will evaluate whether these newer treatments make daily HS or DA unnecessary. The trial begins with a 6-week run-in period where participants continue ETI or VTD but stop using HS and DA. Eligible participants are then assigned to either the HS Study or the DA Study for one year. Within those groups, they are randomized to either daily use of HS or DA or as needed use only during respiratory illnesses. The study aims to find out if lung health is similar between children and teens taking HEMT who use HS or DA treatments daily and those who use HS or DA treatments only when they are sick.

Study identification

NCT ID
NCT07696338
Recruitment status
Not yet recruiting
Study type
Interventional
Phase
Not applicable
Lead sponsor
Nicole Hamblett
Other
Enrollment
405 participants

Conditions and interventions

Eligibility (public fields only)

Age range
3 Years to 16 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Sep 14, 2026
Primary completion
Feb 27, 2030
Completion
Feb 27, 2030
Last update posted
Jul 9, 2026

2026 – 2030

United States locations

U.S. sites
36
U.S. states
24
U.S. cities
35
Facility City State ZIP Site status
The Children's Hospital Alabama, University of Alabama at Birmingham Birmingham Alabama 35233
Tucson Cystic Fibrosis Center Tucson Arizona 85724
Childrens Hospital Los Angeles Los Angeles California 90027
CHOC Children's Hospital Orange California 92868
Stanford University Medical Center Palo Alto California 94025
Children's Hospital Colorado Aurora Colorado 80045
All Children's Hospital St. Petersburg Florida 33701
Children's Healthcare of Atlanta and Emory University Atlanta Georgia 30322
Ann & Robert H. Lurie Children's Hospital of Chicago Chicago Illinois 60611
Riley Hospital for Children Indianapolis Indiana 46202
University of Iowa Iowa City Iowa 52242
John Hopkins Hospital Baltimore Maryland 21287
Boston Children's Hospital Boston Massachusetts 02115
University of Michigan, Michigan Medicine Ann Arbor Michigan 48109
Children's Hospitals and Clinics of Minnesota Minneapolis Minnesota 55404
The Minnesota Cystic Fibrosis Center Minneapolis Minnesota 55455
Children's Mercy Kansas City Kansas City Missouri 64108
St. Louis Children's Hospital St Louis Missouri 63110
University of Rochester Medical Center Strong Memorial Rochester New York 14642
University of North Carolina at Chapel Hill Chapel Hill North Carolina 27599
Cincinnati Children's Hospital Medical Center Cincinnati Ohio 45229
Rainbow Babies and Children's Hospital/University Hospitals Cleveland Medical Center Cleveland Ohio 44106
Nationwide Children's Hospital Columbus Ohio 43205
Dayton Children's Hospital Dayton Ohio 45404
Oregon Health & Sciences University Portland Oregon 97239
Children's Hospital of Philadelphia Philadelphia Pennsylvania 19104
Children's Hospital of Pittsburgh of UPMC Pittsburgh Pennsylvania 15224
Medical University of South Carolina Charleston South Carolina 29425
University of Texas Southwestern / Children's Health Dallas Texas 75207
Baylor College of Medicine Houston Texas 77030
University of Virginia Charlottesville Virginia 22904
Virginia Commonwealth University Richmond Virginia 23219
Seattle Children's Hospital Seattle Washington 98105
Providence Medical Group, Cystic Fibrosis Clinic - Pediatrics Spokane Washington 99204
University of Wisconsin Madison Wisconsin 53792
Children's Wisconsin Milwaukee Wisconsin 53226

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 3 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT07696338, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jul 9, 2026 · Synced Sep 4, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT07696338 live on ClinicalTrials.gov.

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