A comparative study of EPINEXUSTM and Commercial Skin Adhesive in patients undergoing surgery: Single Center, Open-Label, Parallel Group Study

A comparative study of EPINEXUSTM and Commercial Skin Adhesive in patients undergoing surgery: Single Center, Open-Label, Parallel Group Study - Clinical comparative study of EPINEXUSTM and Commercial product

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000016753

Enrollment

Registered

2015-03-15

Start date

2015-08-01

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

operation wouund

Interventions

wound closure with EPINEXUSTM for incision wound wound closure with Commercial Skin Adhesive for incision wound

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Patient who receive tumor resection by plastic surgeon or breast surgeon

Exclusion criteria

Exclusion criteria: allergy for methyl methacrylate skin disease keloid

Design outcomes

Primary

Measure	Time frame
cosmetic outcome of wound	—

Secondary

Measure	Time frame
wound closure rate usability	—

Countries

Japan

Contacts

Public ContactNoriko Aramaki

Keio university, school of medicine Plastic and reconstructivve surgery

nonken@2001.jukuin.keio.ac.jp03-5363-3814

Outcome results

None listed

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