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Innervated Sensory Cross-Finger Flap

The Innervated Sensory Cross-finger Flap Based on the Dorsal Branch Artery for Reconstruction of Fingertip Degloving Injury

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01019811
Acronym
ISCF
Enrollment
16
Registered
2009-11-25
Start date
2001-05-31
Completion date
2008-05-31
Last updated
2009-11-25

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

Conditions

Transplantation

Keywords

Cross-finger flap, finger injuries, fingertip reconstruction, proper digital artery, proper digital nerve.

Brief summary

The purpose of this study is to introduce a new operative technique for reconstruction of fingertip degloving injury.

Detailed description

Incidence of fingertip degloving injury is common and can result in functional morbidity. A cross-finger flap based on the dorsal branch artery (DBA) including sensory nerve is a useful reconstructive technique.In our modification, the innervated sensory flap is vascularized by the DBA, both its pedicle is narrow and its coverage is extended, the projecting tip of exposed distal phalanx of adjacent digits therefore can be wrapped.

Interventions

PROCEDUREThe innervated sensory cross-finger flap

The innervated sensory cross-finger flap is a modified method for repair fingertip degloving injury

Sponsors

The Second Hospital of Tangshan
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
12 Years to 59 Years
Healthy volunteers
No

Inclusion criteria

* the fingertip degloving injury including the thumb; * age between 12 and 59 years; * no life-threatening associated injuries.

Exclusion criteria

* age greater than 60 years; * smoking; * Dupuytren's contracture; * peripheral arterial disease and other vascular disorders.

Design outcomes

Primary

MeasureTime frame
static 2-point discrimination test and the range of motion are used for evaluation of outcomesat least 4 months

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026