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A retrospective study analyzing the efficacy of medication and microneedling in the treatment of rosacea

A retrospective study analyzing the efficacy of medication and microneedling in the treatment of rosacea

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400087070
Enrollment
Unknown
Registered
2024-07-18
Start date
2023-07-08
Completion date
Unknown
Last updated
2024-07-22

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

Conditions

Rosacea

Interventions

Doxycycline treatment group:NA
Microneedles-aided bloodletting therapy group :NA

Sponsors

Xiangya Hospital Central South University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 55 Years

Inclusion criteria

Inclusion criteria: (1) Females or males aged 18-55 years; (2) Patients diagnosed with rosacea based on the International Diagnostic Criteria for Rosacea(2017) ; and patients with rosacea predominantly of the erythematous capillary dilatation type based on the International Committee of Rosacea Experts(2002) typing; (3) Those who had taken oral doxycycline 0.1g 1/night for 3 months in our hospital, with unsatisfactory therapeutic effect or recurring condition, underwent microneedling treatment in our hospital 1 time/month 3 times; (4) Subjects who accept retrospective collection of clinical data and can provide portraits; (5) Understanding and willing to participate in this clinical study and voluntarily signing the informed consent form (all satisfied to be included).

Exclusion criteria

Exclusion criteria: 1) Had rosacea-related pustules; 2) Lacks of rosacea-related data (images or self-reported symptoms) before or after DXC treatment; 3) Had severe systematic diseases which could affect the outcome of this trial; 4) Pregnant of lactating women; 5) Had other facial skin disorders (e.g., psoriasis, eczema, infection); 6) Had coagulation disorders and/or bleeding tendency; 7) Underwent any treatment for rosacea in the past one month; 8) Unable/Unwilling to follow-up.

Design outcomes

Primary

MeasureTime frame
Clinician's Erythema Assessment (CEA);

Secondary

MeasureTime frame
the Investigator's Global Assessment (IGA) scale of papule;Capillary dilatation (percentage of dilated capillary area/total facial area));Swelling ;flushing ;burning ;dryness ;itching ;Dermatology Life Quality Index (DLQI);hemorheologic ;

Countries

China

Contacts

Public ContactDan Jian

Xiangya Hospital Central South University

jiandan@csu.edu.cn+86 137 8711 7041

Outcome results

None listed

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