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Analysis of Subcutaneous Fluid Collection After PEEK Material Cranioplasty

Analysis of Subcutaneous Fluid Collection After PEEK Material Cranioplasty

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500100504
Enrollment
Unknown
Registered
2025-04-10
Start date
2025-04-10
Completion date
Unknown
Last updated
2025-04-14

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

Conditions

Skull defects

Interventions

The group with subcutaneous effusion after repair surgery:None
The group without subcutaneous effusion after repair surgery:None

Sponsors

China Rehabilitation Research Center(Beijing Bo'ai Hospital)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.Patients who successfully underwent PEEK cranial repair in this center. 2. Follow - up for one year.

Exclusion criteria

Exclusion criteria: 1.Patients with bilateral cranial repair using titanium mesh on one side and PEEK material on the other side.

Design outcomes

Primary

MeasureTime frame
Subcutaneous effusion;—

Countries

China

Contacts

Public ContactJianjun Wang

China Rehabilitation Research Center(Beijing Bo'ai Hospital)

wangjianjun00001@163.com+86 10 87569051

Outcome results

None listed

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