Clinical trial of acellular dermal matrix in prevention of postoperative tendon adhesion.

Clinical trial for the efficacy and safety of acellular dermal matrix in prevention of postoperative tendon adhesion following tendon repair.

Status

Recruiting

Phases

Phase 4

Study type

Interventional

Source

CRIS

Registry ID

KCT0004104

Enrollment

Registered

2019-06-28

Start date

2018-10-29

Completion date

Unknown

Last updated

2019-07-17

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

Conditions

None listed

Interventions

Medical Device : In Tendon Repair Operation, 1. Control : No application 2. Case : ADM (Acellular dermal matrix application)

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: - over 19 years old - flexor tendon injury zone I,II, distal to palmar digital crease - within 48 hours after injury - index, middle, ring, little finger injury

Exclusion criteria

Exclusion criteria: - history of trauma in same hand - underlying general disease (RA, OA, SLE) - over two tendons injury

Design outcomes

Primary

Measure	Time frame
TAM (total active motion)	—

Secondary

Measure	Time frame
Period after TAM reaches 75% compared to normal value	—

Countries

Korea, Republic of

Contacts

Public ContactHyung-Sup Shim

The Catholic University of Korea

sharpshim@yahoo.co.kr+82-31-249-7206

Outcome results