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Postoperative Skin Surface Tension Relaxing in Prevention of Facial Surgical Skin Scarring

NCT03842644 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 55

Last updated 2020-10-29

No results posted yet for this study

Summary

The purpose of this study is to evaluate the efficacy and safety of early postoperative skin surface reduction in improving scar formation after facial surgery.

Conditions

  • Scar

Interventions

DEVICE

Tension reduction device

Continue using this device for 3 months post surgery.

Sponsors & Collaborators

  • XiaoXi Lin

    lead OTHER

Principal Investigators

  • Lin, Professor · Shanghai Ninth People's Hospital Affiliated to Shanghai Jiao Tong University

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
6 Years
Max Age
40 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-02-16
Primary Completion
2020-10-25
Completion
2020-10-25

Countries

  • China

Study Locations

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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 NCT03842644 on ClinicalTrials.gov