TEOSYAL RHA® 1 for Neck Lines, Perioral Lines and Smiling Lines
Status
Conditions
Treatments
Details and patient eligibility
About
Prospective, low-interventional, multicentric, open-labelled study to assess the performance and safety of skin beautification treatment by TEOSYAL RHA® 1 for fine lines in the neck, perioral region, and smiling lines including an exploratory arm with TEOSYAL® PureSense Redensity 1 to assess skin redensification.
Treatment phase - skin beautification:
At Visit 1 (Baseline), subjects will be injected with TEOSYAL RHA® 1 in the fine lines (Neck lines and Perioral and/or Smiling lines) depending on wrinkle severity assessed by the Principal Investigator (PI) at baseline using a specific grading scale for each indication.
The subject will be included in the study if he has been graded 2 or 3 on the Neck Lines Descriptive Scale (NLDS) at baseline.
Then:
- The subject will be included in the perioral rhytids cohort if he has been graded 2 or 3 on the Perioral Rhytids Severity Rating Scale (PR-SRS) at baseline.
- The subject will be included in the smiling lines cohort if he has been graded 3 or 4 on the Smiling Lines Descriptive Scale (SLDS) at baseline.
Each indication represent one cohort and all subjects will be included in the neck lines cohort.
Thus, Subject participating to the study may be treated for:
- Neck Lines and perioral Lines (2 cohorts)
- Neck Lines and Smiling Lines (2 cohorts)
- Neck Lines, Perioral Lines and Smiling Lines (3 cohorts)
An optional touch-up will be performed at Visit 2 (Month 1 +/- 1 week) if deemed necessary to achieve an optimal correction.
Exploratory phase - skin redensification:
After treatment with TEOSYAL RHA® 1, subjects will be randomized to the second phase of the study (starting at month 2 +/- 1 week): 5/6 of the subjects will enter the exploratory part of the study during which TEOSYAL® PureSense Redensity 1 (RHA1+R1 treated Group) will be assessed for skin redensification. The rest of the subjects will not receive any additional treatment for the rest of the study (RHA1 only treated group/around 11 subjects).
Note: the number of sessions treated with Redensity 1 might be adapted depending on subject treatment needs in order to achieve optimal results. This will be at PI discretion.
Subjects in the RHA+R1 treated Group will be also randomized into 2 subgroups of 28 subjects as described below:
- Sub-Group A: injection with a needle for all indications
- Sub-Group B: injection with a cannula for neck lines and smiling lines indications* *The perioral indication will be treated with a needle for this group.
The principal investigator (PI) will perform the study injections. He will evaluate subject aesthetic improvement using grading scales and skin quality measurements at each study visits and assess safety and tolerability of the devices during the study. Adverse events will be monitored by the Clinical Research Associate (CRA) throughout the study.
Additionally, a Blinded Evaluator will also evaluate subject aesthetic improvement using grading scales for each follow-up visits based on photographs.
Enrollment
Sex
Ages
Volunteers
Inclusion and exclusion criteria
Inclusion Criteria (General):
- Healthy adults, 35 to 70 years old seeking an improvement of their aesthetic appearance and beautification of their skin in 3 areas: perioral lines, smiling lines and neck lines.
- Subjects having given their informed consent.
- Subjects having wrinkle severity ranked as mild to moderate neck lines (grade 2 or grade 3 on the NLDS)
Inclusion Criteria (Cohort) 4. Healthy adult having wrinkle severity in at least one of the two indications (50% for each of the following cohort): i. Moderate to severe perioral rhytids (grade 2 or grade 3 on the PR-SRS) ii. Moderate to severe smiling lines (grade 3 or grade 4 on the SLDS)
Exclusion Criteria:
- Minor subjects
- Subjects who already had fillers and/or other skin quality treatment(s) in the 6 months preceding the study.
- Subjects undergoing or planning to undergo peeling treatment or laser/ultrasound-based treatment during the study or having had one of these treatments in the 6 months preceding the study.
- Subjects showing cutaneous disorders, inflammation or infection (acne, herpes, scars...) at the treatment site or near to this site.
- Subjects having a known hypersensibility to lidocaine and/or amide local anesthetic agents or hyaluronic acid, or with history of severe allergy or anaphylactic shock.
- Subjects with autoimmune or cardiac diseases and/or undergoing treatment for heart diseases (beta blockers).
- Subjects with hepatocellular insufficiency and/or undergoing treatment for liver disease.
- Subjects suffering from epilepsy or porphyria.
- Subjects with severe, ongoing and/or uncontrolled disease that may pose a health risk to the subject during the study and/or may have an impact on the study assessments.
- Subjects receiving or planning to receive high dose Vitamin E, aspirin, anti-inflammatories, or anti-coagulant during the week preceding each injection.
- Subjects receiving any long-term medical treatment or any treatment that, in the opinion of the clinical investigator, may interfere with test results or put the subject at undue risk.
- Subjects under guardianship/tutorship.
- Pregnant women or breastfeeding mother.
- Subjects participating to another research on human beings or being in an exclusion period for a previous study.
Trial design
Primary purpose
Allocation
Interventional model
Masking
67 participants in 3 patient groups
Trial contacts and locations
There are currently no registered sites for this trial.
Timeline
Last updated: May 04, 2022Start date
Oct 05, 2021 • 3 years ago
End date
Dec 13, 2021 • 3 years ago
Today
May 06, 2025
Sponsor of this trial
Lead Sponsor
Data sourced from clinicaltrials.gov
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