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PER-SAF_PDOS (Performance and Safety of Polydioxanone Suture)

NCT07068061 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 50

Last updated 2025-07-16

No results posted yet for this study

Summary

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.

Conditions

  • Wrinkles
  • Anti Aging
  • Face-lift

Interventions

DEVICE

PDO suture

A biodegradable polymer used in dissolvable sutures and lifting threads, stimulating collagen production as it degrades.

Sponsors & Collaborators

  • 21 Century Medical Co., Ltd.

    lead INDUSTRY

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-09-01
Primary Completion
2026-07-01
Completion
2026-07-01

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07068061 on ClinicalTrials.gov