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NCT05042258RecruitingPhase 4

Using Dupilumab to Improve Circadian Function, Sleep and Pruritus in Children With Moderate/Severe Atopic Dermatitis

Source: ClinicalTrials.gov · Last updated 27 Apr 2026

Brief summary (registry, in English)

Single center, prospective, Open label study of sleep, pruritus and circadian function pre/post 12-weeks of dupilumab treatment in children 6-17 years old

Status (registry)
Recruiting
Phase (registry)
Phase 4
Study type
Interventional
Enrollment
40 (estimated)
First submitted
27 Jul 2021
Start date
12 Aug 2024
Primary completion date
30 Jun 2027
Lead sponsor
Northwestern University
NCT number
NCT05042258

What you commit to

  • Study type: Interventional · Phase 4
  • Planned participants: 40
  • From 12 Aug 2024 to the primary completion date, 30 Jun 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Use of concomitant medication that causes scratching.
  • Having applied topical steroids within 7 days of first or second PSG (important for biomarkers assessment).
  • Other contraindication to receiving dupilumab (such as history of allergic reaction to dupilumab or any of its components).

Other illness

  • Self-reported sleep disturbance on 2 or more nights in the past 7 days due to allergic rhinitis.
  • Major medical condition (such as cancer).
  • Active condition that could affect sleep, such as obstructive sleep apnea, restless leg syndrome, insomnia, narcolepsy, severe sleep disordered breathing, severe depression, COVID-19, or hives (urticaria).

Other

  • Poorly controlled asthma (Asthma Control Test ≤19).
  • Use of systemic immunosuppressant within 30 days of first PSG.
  • Having showered or used moisturizers within 12 hours of first or second PSG.
  • Unable to communicate in English (some PROMIS questionnaires not available in translation).
  • Pregnancy.
  • Clinical blindness (circadian disturbing).

Who the study is looking for

  • Participants, 6-17 years old at time of enrollment.
  • Moderate to severe chronic AD inadequately controlled by topical treatment, diagnosed according to Hanifin and Rajka criteria by a pediatric dermatologist or allergist.
  • AD severity will be determined at baseline with Validated Investigator Global Assessment (vIGA) score of moderate (3) or severe (4).
  • Patient assessed or parent-proxy (under 8 years old) PROMIS sleep disturbance T-score ≥60.
  • Willing and able to comply with visits and study-related procedures.
  • On stable regimens (consistent use 14 days before Day 1 of study enrollment) of inhaled corticosteroids, topical steroids, and antihistamines.

Age in the registry: 6 years to 17 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Lurie Children's Hospital/Northwestern University
Coordinator of this site? Confirm its status
ChicagoUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.