Status:
COMPLETED
FMRF Combined With 30% SSA in the Treatment of Rosacea
Lead Sponsor:
Second Affiliated Hospital of Xi'an Jiaotong University
Conditions:
Rosacea
Eligibility:
All Genders
18-60 years
Phase:
NA
Brief Summary
This study was a single-center, case-by-case, bilateral facial comparison study. A total of 15 patients were included. On the day of enrollment, after the completion of the test items, treatment was c...
Detailed Description
This study is a single-center case-control study with half-side face as the control group. According to the inclusion and exclusion criteria, 15 patients with rosacea (erythema and telangiectasia type...
Eligibility Criteria
Inclusion
- According to the latest diagnostic criteria of the American Rosacea Society (2017 version) - Annex 1, patients diagnosed with the main phenotype of erythema and telangiectasia.
- The therapeutic response to the medication is unsatisfactory and the condition is prone to relapse.
- Age range: 18 to 60 years old
- The patient voluntarily participated in this clinical study and signed the written informed consent form.
Exclusion
- The patient has other skin disorders on the face, such as melasma, freckles and seborrheic dermatitis, which may affect the judgment of the test results.
- Individuals who are allergic to the test drug or have hypersensitive constitution.
- Patients who are pregnant, about to become pregnant or are lactating.
- Patients with acne during the consultation.
- Patients who had undergone facial injections or surgeries within the past two months before the trial.
- Patients with immunodeficiency diseases and abnormal coagulation function.
Key Trial Info
Start Date :
December 1 2023
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
November 14 2024
Estimated Enrollment :
15 Patients enrolled
Trial Details
Trial ID
NCT06969300
Start Date
December 1 2023
End Date
November 14 2024
Last Update
May 13 2025
Active Locations (1)
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1
The Second Affiliated Hospital of Xi'an Jiaotong University
Xi'an, Shaanxi, China, 710000