Actively Recruiting

Age: 18Years +
All Genders
Healthy Volunteers
NCT07573735

Assessment of cfDNA-STING Axis as a Potential Pathological Marker in Atopic Dermatitis

Led by Zhongda Hospital · Updated on 2026-05-07

80

Participants Needed

1

Research Sites

17 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Study Overview Atopic dermatitis (AD), commonly known as eczema, is a chronic inflammatory skin condition characterized by intense itching and skin barrier damage. While researchers know that the immune system is overactive in AD, it is difficult to measure the exact level of "damage" or "inflammation" happening deep within the skin using only a physical exam. The Purpose of This Study This study investigates a specific "danger signal" called circulating cell-free DNA (cfDNA). When skin cells are damaged or die due to inflammation, they release tiny fragments of DNA into the bloodstream. We believe these fragments might act as a trigger for the immune system, worsening the disease. What the Study Involves Researchers will collect blood samples and small skin biopsies from patients with AD and healthy volunteers. The study aims to: Compare the levels of cfDNA in the blood of AD patients versus healthy individuals. Determine if higher levels of cfDNA correlate with more severe skin symptoms (measured by scores like SCORAD and EASI). Examine how immune cells in the skin (macrophages) respond to these DNA fragments through a specific biological switch called the STING pathway. Potential Impact By understanding this "damage-signal" loop, this research may lead to new ways for doctors to monitor AD severity through simple blood tests and could identify new targets for future anti-inflammatory treatments.

CONDITIONS

Official Title

Assessment of cfDNA-STING Axis as a Potential Pathological Marker in Atopic Dermatitis

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients aged older than 18 with a confirmed diagnosis of AD and visible skin lesions.
Not Eligible

You will not qualify if you...

  • Patients who have received systemic immunosuppressants, systemic corticosteroids, or biological agents (e.g., Dupilumab) within the past 4 weeks.
  • Patients who have used topical treatments within the past 2 weeks to avoid interference with inflammatory markers.

AI-Screening

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Trial Site Locations

Total: 1 location

1

Zhongda Hospital, Southeast University

Nanjing, Jiangsu, China

Actively Recruiting

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How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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