PER-SAF_PDOS (Performance and Safety of Polydioxanone Suture)
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
Sponsor21 Century Medical Co., Ltd.
About this trial
This clinical investigation aims to confirm the safety and efficacy of the ID in facial soft tissue reconstruction, specifically for non-incision surgery to tighten and lift the facial skin for a rejuvenated facial appearance.
Eligibility criteria
Qualifiers
Patients over 18 years old with full legal capacity, male and female;
Patients with ability to understand the proposed aesthetic correction and to understand and sign informed consent;
Patients who are willing and able to comply with scheduled visits, aesthetic correction procedure and other trial procedures.
Disqualifiers
Pregnant or breast--feeding women;
Patients currently participating in any other clinical investigation;
Patients who have received a vaccine within 14 days prior to the baseline or plan to have vaccine within 14 days after the injection;
Patients with a medical history of systemic diseases, including severe kidney, liver, heart and neurological disorders.
Trial design
Treatments tested in this trial
- PDO suture
Treatment groups
50 Participants
are divided into 1 treatment groupLocations
Sponsors and collaborators
Source ClinicalTrials.gov