Please sign in to follow a disease.
New combo treatment targets Crow's feet and hollow eyes
NCT ID NCT07398755
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This completed study observed 29 adults receiving a combination of botulinum toxin (Letybo), hyaluronic acid filler (Saypha Volume Plus), and polynucleotide injections (Philart Eye) around the eyes. The goal was to see how well this holistic approach reduces wrinkles and restores volume over 22 weeks. Researchers measured skin changes and patient satisfaction at several follow-up visits.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- botulinum toxin A, hyaluronic acid filler, and polynucleotide
- What this could lead to
- If successful, this could confirm that a combination of these injectable treatments safely improves wrinkles and volume loss around the eyes for several months.
- What could go wrong
- This is a small, completed observational study with only 29 participants. Results may not apply to everyone, and the effects are temporary, requiring repeat treatments.
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
-
29 people
The number who actually took part.
- Started
-
Sep 2025
- Finished
-
Mar 2026
- Lead sponsor
-
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
Patients visiting the clinic for such a treatment as part of routine clinical practice.
- Ages
-
18 to 75 years
- Sex
-
Anyone
- Healthy volunteers
-
Accepted
You do not need to have the condition being studied to take part.
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: 1. 18 years or older at time of treatment. 2. At least mild periorbital skin wrinkling, mild frown lines at maximum frown and mild. midface volume deficiency as assessed by the investigator 3. Subject has a stable medical condition with no uncontrolled systemic disease. 4. Willingness to participate in the routine follow-up after 8 weeks and 22 weeks and a signed informed consent form. 5. Subject already visiting the clinic for the specific treatment. Exclusion Criteria: 1. Pregnancy and breast feeding. 2. Neuromuscular disease (e.g. myasthenia gravis, Eaton - Lambert syndrome). 3. Known impairment of blood coagulation. 4. Drooping eyelid. 5. Known allergy to botulinum toxin or human albumin (blood protein). 6. Presence of acute infection or inflammation at the proposed injection sites. 7. Botulinum toxin treatment in the glabella within the last 16 weeks. 8. HA- Filler treatment in the midface or periorbital area within the last 6 months. 9. Patients with a history of autoimmune disease or who are receiving immune therapy. 10. History of hypersensitivity to hyaluronic acid, lidocaine hydrochloride or other amidetype local anaesthetics. 11. History of fish product allergy.
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Glabellar lines are added.
Genom att skicka in godkänner du våra Användarvillkor
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
YUVELL
Vienna, State of Vienna, 1010, Austria
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Can a new injection smooth away frown lines?
- Can a One-Two injection punch smooth frown lines better?
- New wrinkle treatment aims to rival botox in Head-to-Head trial
- New wrinkle treatment shows promise in asian trial
- New frown line combo treatment under study
- New Frown-Line treatment shows promise in large trial