Evaluation of Absorbable Screw-Assisted Wound Closure for Scalp Defects: A Randomized Controlled Trial

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0010786

Enrollment

Registered

2025-07-17

Start date

2025-09-01

Completion date

Unknown

Last updated

2025-07-21

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

Conditions

None listed

Interventions

Procedure/Surgery : This study is a randomized controlled clinical trial comparing the efficacy and safety of a screw-assisted closure method using absorbable Fixtine screws versus the conventional tw

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1. Adults between 18 and 79 years of age, inclusive. 2. Patients with scalp wounds (e.g., defects after tumor removal, lacerations). 3. Individuals with a wound expected to be 3 cm or longer after defect closure. 4. Those who have provided informed consent to participate in the study.

Exclusion criteria

Exclusion criteria: 1. Patients with active infection. 2. Patients who are taking immunosuppressants or have compromised immune function. 3. Individuals with a history of complications from previous wound treatments.

Design outcomes

Primary

Measure	Time frame
Scar Quality Assessment	—

Secondary

Measure	Time frame
Surgical Efficiency;Safety and Complication	—

Countries

Korea, Republic of

Contacts

Public Contactyoungchul Kim

Asan Medical Center

youngchulkk@naver.com+82-2-3010-1250

Outcome results