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Correlation analysis study of skin and ocular microecology and metabolomics in rosacea

Correlation analysis study of skin and ocular microecology and metabolomics in rosacea

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500112466
Enrollment
Unknown
Registered
2025-11-14
Start date
2025-12-20
Completion date
Unknown
Last updated
2025-11-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Rosacea

Interventions

Simple rosacea skin type group:None
Rosacea with manifestations on both the skin and the eyes group:None
Only ocular meibomian gland dysfunction (MGD) group:None

Sponsors

Bejing Tongren Hospital, Capital Medical Uniersity
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Voluntarily participate in this clinical study and sign the informed consent form; 2. No gender restriction, age between 18 and 70 years old; 3. (1) Rosacea with only skin involvement group: skin manifestations meet the diagnostic criteria for rosacea; (2) Rosacea with both skin and ocular involvement group: skin manifestations meet the diagnostic criteria for rosacea, and ocular findings confirmed by an ophthalmologist meet the criteria for ocular rosacea; (3) Meibomian gland dysfunction only group: no skin disease, and ocular findings confirmed by an ophthalmologist meet the criteria for meibomian gland dysfunction; (4) Healthy control group: no skin disease and no ocular disease.

Exclusion criteria

Exclusion criteria: 1. Use of systemic medications within the past 3 months, or topical antibiotics, antiparasitic, or anti-inflammatory steroid treatments within the past 2 weeks; 2. Presence of other skin diseases on the face besides rosacea, or currently using other treatments for rosacea; 3. Patients with other systemic diseases that make them unsuitable for enrollment (such as confirmed gastrointestinal diseases (e.g., IBD), autoimmune diseases, tumors, uncontrolled hypertension or diabetes, etc.); 4. Pregnant or breastfeeding women; 5. Patients who have smoked within the past 3 months or consumed alcohol within the past week (excluding chronic alcoholics); 6. Patients with significant abnormalities observed under slit-lamp examination and/or deemed by the investigator to potentially affect the assessment of eyelid margin inflammation-related indicators, including ocular trauma or history of ocular trauma, eyelid anatomical abnormalities, etc.; 7. Patients who have received local treatments on the eyes with tea tree oil, okra eye patches, or hypochlorous acid within the past 2 weeks, or those with a history of intraocular surgery or trauma. Patients who have worn contact lenses or used corticosteroid or antibiotic eye drops in the past month; 8. Used eyelid cleaning products (e.g., eyelid cleansing solution) within 2 weeks, or unwilling to discontinue use of eyelid cleaning products during the study. Used false eyelashes, eyelash extensions, or other cosmetic eyelash or eyelid procedures (e.g., eyeliner tattooing, eyelash tinting, eyelash perming, etc.) within 1 week, or unwilling to discontinue use during the study; 9. Received intense pulsed light (IPL) treatment, such as optimized pulse technology (OPT) or intense regulated pulsed light (IRPL) within 2 weeks, or unwilling to discontinue these treatments during the study; 10. Active eye allergies or ocular or systemic infections (bacterial, viral, or fungal), including fever. Conditions that may, or are deemed by the investigator to, pose significant risk to the subject, confound trial results, or severely interfere with the subject’s participation in the study (including language barriers). Presence of ocular or periocular malignant tumors; 11. Patients who have not signed the informed consent form.

Design outcomes

Primary

MeasureTime frame
Meibomian gland function, secretion capacity and nature score;Skin Quality of Life Score (DQLI Score);OSDI;The severity of rosacea lesions;Microscopic examination of Demodex eyelashes;

Secondary

MeasureTime frame
Tear film lipid layer thickness;Corneal fluorescence staining score;TMH /tear meniscus height;Schirmer test under non-anesthetic conditions;Facial mite examination;Eyelid margin physical sign score;breakup time of tear film;

Countries

China

Contacts

Public ContactTao Rong

Bejing Tongren Hospital, Capital Medical Uniersity

Jennifertao112@163.com+86 10 58268092

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026