Comparative study of surgical scar and complications with different suture strings

Comparative study of surgical scar and complications with different suture strings - Comparative study of surgical scar and complications with different suture strings

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000005075

Enrollment

Registered

2011-02-14

Start date

2011-02-01

Completion date

Unknown

Last updated

2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

examination of surgical scar and complications with different suture strings

Interventions

A group: Surgical wound is divided in half.The upper part is sutured with PDS and the lower part is sutured with V-Loc 180. B group: Surgical wound is divided in half.The upper part is sutured with

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1,Written informed consent. 2,Surgical wound was 10cm or more.

Exclusion criteria

Exclusion criteria: 1,Clinically significant infectious disease. 2,Emergency surgery 3,Patients who are considered unsuitable for this study by the investigator. 4,Surgical wound was less than 10cm.

Design outcomes

Primary

Measure	Time frame
The comparison between postoperative scar and complications. Based on a clinical photograph ( post 1 month, post 3 months, post 6 months, post 1 year), we evaluate the difference with the surgical scar, the difference with suture strings.	—

Secondary

Measure	Time frame
wound complications hypertrophic scar Aesthetics wound closure time cost	—

Countries

Japan

Contacts

Public ContactToshiyuki Ozawa

Osaka City University Department of Plastic and Reconstructive Surgery

ozawa@med.osaka-cu.ac.jp06-6645-3892

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026