Dermatologists unite to end skin booster chaos!
NCT ID NCT07296601
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study brings together 15 skin experts to agree on the best ways to use skin boosters—injections that improve skin hydration and texture. The goal is to create clear, practical guidelines for doctors, covering who should get them, how to inject, and safety tips. Participants are experienced dermatologists, not patients, and the study does not test any new treatment.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 15 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Dec 2025
An estimate. Start dates often move.
- Expected to finish
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Jan 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
The study population will consist of a purposively selected panel of experts in aesthetic dermatology and skin booster therapy. Participants will include board-certified dermatologists, aesthetic physicians, and plastic surgeons with substantial clinical experience in administering injectable skin quality treatments. The expert panel will represent a diverse range of clinical backgrounds, geographical regions, and practice settings to ensure comprehensive and balanced perspectives.
- Ages
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Children (under 18), adults (18 to 64) and older adults (65 and over)
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Inclusion Criteria Experts will be eligible to participate if they meet all of the following: Board-certified dermatologist or aesthetic physician With recognized qualification in dermatology, aesthetic medicine, plastic surgery, or related fields. Minimum clinical experience At least 5 years of experience performing aesthetic injectable procedures. OR at least 3 years of consistent use of skin boosters in clinical practice. Demonstrated expertise in skin booster therapy Must have performed ≥100 skin booster procedures overall, OR ≥20 sessions per year over the past 2 years. Active clinical practice Currently practicing in an aesthetic or dermatology clinic, medical center, or hospital. Authorship or contribution to aesthetic/dermatology education (desirable but not mandatory) Publications, lectures, workshop instruction, or conference involvement in aesthetics. Ability to participate in Delphi rounds Must agree to complete all survey rounds within the specified timeframe. Must be fluent in the language used for the study (e.g., English or Arabic). Willingness to provide informed consent Voluntary participation with confidentiality maintained. Exclusion Criteria: * Less than the required experience \<5 years of aesthetic practice OR insufficient hands-on experience with skin booster injections. Limited familiarity with skin booster products or techniques No regular use in the last 2 years. Has not performed the minimum number of required procedures. Industry conflict of interest Direct employment by a company manufacturing skin booster products. Significant financial relationship with a single product manufacturer that may bias responses. Inability to commit to multiple Delphi rounds Anticipated non-compliance or non-response in iterative rounds. Non-clinical or administrative professionals Those not actively practicing (e.g., retired, research-only positions, students, trainees). Participation in a competing guideline project Experts currently serving on another skin booster consensus panel to avoid duplication or bias. Failure to provide informed consent Declines participation or withdraws consent at any time.
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
The full official record for this study. This one lists no contact details, but it is the first place any would appear.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Venus Research Center
Cairo, Egypt
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