Skip to content

A multicenter randomized controlled clinical study of intense pulsed photodynamic therapy for rosacea

A multicenter randomized controlled clinical study of intense pulsed photodynamic therapy for rosacea

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400082753
Enrollment
Unknown
Registered
2024-04-07
Start date
2024-04-15
Completion date
Unknown
Last updated
2024-04-08

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

Conditions

rosacea

Interventions

IPL-PDT group: Patients were instructed to cleanse their faces with water before the application of fresh 5% ALA cream to the lesion area.After 20 minutes of sheltering from light, excess ALA was remo
minocycline group:Oral minocycline, 50mg twice daily for 8 weeks

Sponsors

Shanghai Skin Disease Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1) Patients aged 18 to 65 years without cognitive impairment, regardless of gender; 2) Diagnosis was based on the 2017 rosacea diagnostic consensus; 3) Patients with a confirmed diagnosis of moderate or severe rosacea (Investigator’s Global Assessment [IGA] scored [3 points); 4) Patients were not suitable for medication for various reasons and voluntarily participated and signed informed consent when informed of alternative options and consented to having their lesions photographed.

Exclusion criteria

Exclusion criteria: 1) Patients with a history of allergies to 5-aminolevulinic acid (ALA), porphyria, danru cream, tetracycline antibiotics or photosensitivity; 2) Recent systemic therapy with typical medications within the last 8 weeks, systemic isotretinoin treatment within the last 6 months; 3) Recent use of phototoxic or photosensitivity drugs within the last 2 months; 4) Patients with other facial skin diseases that may confound the evaluation of efficacy; 5) Patients with serious physical or mental illnesses, and pregnant or breastfeeding women.

Design outcomes

Primary

MeasureTime frame
the reduction rate of lesion count;

Secondary

MeasureTime frame
Clinician's Erythema Assessment scale,CEA;RosaQoL;

Countries

China

Contacts

Public ContactXiuli Wang

Shanghai Skin Disease hospital

wangxiuli_1400023@tongji.edu.cn+86 180 1733 6663

Outcome results

None listed

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