Skip to content

The clinical application of semi mattress suture technology in the treatment of ingrained paronychia

The clinical application of semi mattress suture technology in the treatment of ingrained paronychia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600129073
Enrollment
Unknown
Registered
2026-07-30
Start date
2022-09-10
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

ingrained paronychia

Interventions

A group:Winograd surgery group with ordinary suture or no suture
B group:Winograd procedure combined with vertical semi mattress suture group

Sponsors

Beijing Pinggu District Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
10 Years to 85 Years

Inclusion criteria

Inclusion criteria: Select patients aged 10-85 years with clinical diagnosis of grade II or above of embedded paronychia who require surgery.

Exclusion criteria

Exclusion criteria: Exclusion criteria for subjects: patients with grade I ingrown nail paronychia of the foot who do not require surgical treatment, patients with osteomyelitis, other diseases caused by foot toe pain not caused by paronychia, poor physical condition that cannot tolerate surgery, and patients with surgical contraindications.

Design outcomes

Primary

MeasureTime frame
Shape;Pain;

Countries

China

Contacts

Public ContactLiu Xinmin

Beijing Pinggu District Hospital

18733593698@163.com+86 187 3359 3698

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Aug 10, 2026