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Clinical Observation of Botulinum Toxin A Treatment in the Treatment of Rosacea

Clinical Observation of Intradermal Injections With Botulinum Toxin A in the Treatment of Rosacea Erythema Telangiectasia

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06282679
Enrollment
30
Registered
2024-02-28
Start date
2022-04-01
Completion date
2024-06-28
Last updated
2024-02-28

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

Conditions

Rosacea, Botulinum Toxin

Brief summary

the goal of this study is to study the clinical efficacy and safety of botox in the treatment of rosacea.

Detailed description

The main objective is to collect patients and then use different injection volumes of botulinum toxin intradermal injection for the treatment of rosacea erythema telangiectasia, and then to evaluate the clinical efficacy and safety of the treatment.

Interventions

you are asked to return to the hospital for follow-up at weeks 2, 4, 8, and 12

Sponsors

Nanjing First Hospital, Nanjing Medical University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

* Meeting the diagnostic criteria of mild to moderate erythema telangiectasis rosette acne; * more than 18 years old; * to obey the rules of the treatment in the study, and can be followed up for 12 weeks; * informed consent;

Exclusion criteria

* Had received facial cosmetic surgery or botulinum toxin treatment within 6 months before this treatment; * due to systemic diseases such as autoimmune diseases or menopause facial flush; * had allergies botulinum toxin; * pregnant or breastfeeding; * other facial skin or oral disease therapy, including research before 4 weeks rose acne accept other treatment; * With basic neuromuscular diseases (such as myasthenia gravis, amyotrophic lateral sclerosis, etc.); * All landowners 4 weeks before the study whether any oral aminoglycoside drugs, benzodiazepines drugs or muscle relaxants; .Was removed during treatment observation data is not complete, incomplete treatment and patients can't take medication as prescribed.

Design outcomes

Primary

MeasureTime frameDescription
CEA score2.4,8,12 weeksClinical erythema score (CEA) was divided into no, mild, moderate and severe according to the severity of rosacea, corresponding to 0,1,2,3, respectively

Secondary

MeasureTime frameDescription
GAIS score2.4,8,12 weekshe Global Aesthetic Improvement Scale (GAIS) score was assessed by the treating physician on the patient's improvement and was divided into four levels: very improved corresponding, substantial improvement, improvement, no change; Corresponding to the best beauty results, significantly improved but not the best, significantly improved, no change

Other

MeasureTime frameDescription
VISIA red zone score2.4,8,12 weeksVISIA Red zone score The patient's face was photographed by VISIA analyzer and corresponding indicators such as feature index and percentage were recorded
Dermatology Quality of Life Score (DLQI)2.4,8,12 weeksThe Dermatology Life Quality Score (DLQI) is scored by answering multiple questions in which patients self-rate the impact of their current illness on their lives over a period of one week. The answer is divided into four levels, very serious 3 points, severe 2 points, a little 1 point, no 0 points;

Countries

China

Contacts

Primary ContactJie Dai
karry_dj@126.com02552271117

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 7, 2026