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Prospective randomized controlled study of artificial dermis induced graftless techniques and conventional surgical methods in syndactyly release

Prospective randomized controlled study of artificial dermis induced graftless techniques and conventional surgical methods in syndactyly release

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400090444
Enrollment
Unknown
Registered
2024-09-30
Start date
2022-08-29
Completion date
Unknown
Last updated
2024-10-07

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

Conditions

Syndactyly

Interventions

Graft Group:Using free skin grafting technique to cover the soft tissue defect after syndactyly release.
Flap Group:Using the dorsal hexagon island flap without skin graft to treat syndactyly.
Pelnac Group :Using Pelnac artificial dermal layer without skin graft to treat syndactyly

Sponsors

Beijing Jishuitan Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
0.5 Years to 3 Years

Inclusion criteria

Inclusion criteria: Patients diagnosed as congenital syndactyly and meet the following conditions: simple syndactyly (including complete and incomplete simple syndactyly) ; younger than 3 years old; normal blood routine; normal blood coagulation; normal liver and kidney function and systemic examination; full informed consent was obtained and participating in the study was voluntary; both genders.

Exclusion criteria

Exclusion criteria: complex syndactyly; poor general condition; Blood coagulation dysfunction; poor compliance and not agreeing to participate in the study.

Design outcomes

Primary

MeasureTime frame
grade of web creep;

Secondary

MeasureTime frame
scar quality;time-consuming of operation;finger deformity;joint mobility;Nail deformity;finger flexibility;infection rate;

Countries

China

Contacts

Public ContactYang Guo

Beijing Jishuitan Hospital, Capital Medical University

drguoyang@163.com+86 137 0133 2661

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026