CompletedPhase 4

Intradermal BoNT-A Treatment in Erythematotelangiectatic Rosacea

Turkey (Türkiye)30 participantsStarted 2022-11-01

Plain-language summary

Investigation of the effectiveness of intradermal botulinum toxin A treatment in the treatment of erythematotelangiectatic rosacea (ETR) using clinical, biophysical, dermatoscopic and videocapillaroscopy.

Who can participate

Age range

18 Years – 60 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * 18-60 years old * Erythematotelangiectatic rosacea subtype * Willingness to participate in the research and providing informed consent Exclusion Criteria: * Patients under 18 years of age, over 60 years of age * A rosacea subtype other than ETR * History of using topical or systemic medications within the past two weeks due to rosacea or other dermatoses * Known history of autoimmune disease * History of neuromuscular disease * History of facial botulinum toxin injection within the last six months * Reporting allergy to the active ingredient * Pregnant or breastfeeding patients * Patients who do not accept treatment and follow-up

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

Assessment of erythema with Clinician's Erythema Assessment scale

Timeframe: One month

Evaluation of erythema using mexameter

Timeframe: One month

Evaluation of erythema by dermatoscopy

Timeframe: One month

Trial details

NCT IDNCT06331533

SponsorIstanbul Training and Research Hospital

Sponsor typeOTHER_GOV

Study typeINTERVENTIONAL

Primary completion2023-05-01

View on ClinicalTrials.gov More Erythematotelangiectatic Rosacea trials

Who can participate

Age range

18 Years – 60 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.