Using Botox to treat rosacea symptoms
Clinical Observation of Intradermal Injections With Botulinum Toxin A in the Treatment of Rosacea Erythema Telangiectasia
This study is testing if Botox injections can help people with mild to moderate rosacea reduce redness and visible blood vessels.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 30 (estimated) |
| Ages | 18 Years to 60 Years |
| Sex | All |
| Sponsor | Nanjing First Hospital, Nanjing Medical University Academic / other |
| Locations | 1 site (Nanjing, Jiangsu) |
| Trial ID | NCT06282679 on ClinicalTrials.gov |
What this trial studies
This study aims to evaluate the clinical efficacy and safety of botulinum toxin type A injections for treating rosacea, specifically targeting erythema and telangiectasia. Patients diagnosed with mild to moderate rosacea will receive varying volumes of the treatment, and their responses will be monitored over a 12-week period. The study will collect data on both the effectiveness of the injections and any potential side effects experienced by participants.
Who should consider this trial
Good fit: Ideal candidates are adults over 18 with mild to moderate erythema telangiectasia rosacea.
Not a fit: Patients with recent facial cosmetic procedures, certain systemic diseases, or allergies to botulinum toxin may not benefit from this study.
Why it matters
Potential benefit: If successful, this treatment could provide a new effective option for patients suffering from rosacea.
How similar studies have performed: While the use of botulinum toxin for cosmetic purposes is well-established, this specific application for rosacea is relatively novel and has not been extensively tested in prior studies.
Eligibility criteria
Show full inclusion / exclusion criteria
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.
Where this trial is running
Nanjing, Jiangsu
- Jie Dai — Nanjing, Jiangsu, China (Recruiting)
Study contacts
- Study coordinator: Jie Dai
- Email: karry_dj@126.com
- Phone: 02552271117
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.