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RECRUITING

Protocol CAUSE-03 / CHEETAH

NCT06136091 · View on ClinicalTrials.gov ↗

Study Summary

This is a one-year longitudinal, observational study of 250 urban children and adolescents with asthma and 60 without asthma, ages 6-17 years old. Participants with asthma will require daily controller therapy with inhaled corticosteroids ICS (at least Step 2 therapy). Those without asthma cannot have used asthma medications in the year prior to enrollment and cannot demonstrate bronchodilator reversibility at baseline. Phenotypic characteristics will be established at baseline, and the participants will be seen at scheduled visits over 12 months. Each participant will be asked to monitor and self-report cold symptoms and will be asked to complete up to three cold visits

Conditions Studied

Study Locations (8)

Massachusetts

  • Boston University School of Medicine: Pulmonary Center — Boston
  • Boston Children's Hospital: Department of Immunology — Boston

New York

  • Icahn School of Medicine at Mount Sinai: Division of Clinical Immunology, Immunology Institute — New York
  • Columbia University Medical Center: Division of Pediatric Pulmonology — New York

Colorado

  • Children's Hospital Colorado: Allergy Program — Aurora

District of Columbia

  • Children's National Medical Center: Children's Research Institute — Washington D.C.

Illinois

  • Ann & Robert H. Lurie Children's Hospital of Chicago: Division of Allergy and Immunology — Chicago

Ohio

  • Cincinnati Children's Hospital Medical Center: Asthma Center — Cincinnati

Trial Details

FieldValue
Enrollment Target 310 participants
Start Date 2024-04-23
Est. Completion 2027-05-01

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06136091

The ClinicalTrials.gov registry entry for NCT06136091 describes a study currently listed as recruiting. It is categorized as an unspecified phase, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 310 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is National Institute of Allergy and Infectious Diseases (NIAID), which has 1,295 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Asthma appearing as the primary indexed condition, and to 0 interventions. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT06136091 reports 8 study locations spanning 6 distinct geographic areas — top geographies include Massachusetts, New York, Colorado. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT06136091 about?

NCT06136091 is a clinical study titled "Protocol CAUSE-03 / CHEETAH". This is a one-year longitudinal, observational study of 250 urban children and adolescents with asthma and 60 without asthma, ages 6-17 years old. Participants with asthma will require daily controller therapy with inhaled corticosteroids ICS (at least Step 2 therapy). Those without asthma cannot h...

What is the current status of trial NCT06136091?

This trial is currently recruiting. The enrollment target is 310 participants. The study started on 2024-04-23. Estimated completion is 2027-05-01.

What conditions does trial NCT06136091 study?

This clinical trial studies the following conditions: Asthma. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

Who is sponsoring clinical trial NCT06136091?

This trial is sponsored by National Institute of Allergy and Infectious Diseases (NIAID), which has 1,295 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06136091 being conducted?

This trial has 8 study locations across Colorado, District of Columbia, Illinois, Massachusetts, New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

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