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The Impact of Modified Suspension Procedure on Postoperative Effusion in PEEK Cranioplasty: A Retrospective Cohort Study

Clinical Application Study on Structural Reconstruction of PEEK Cranioplasty and Prevention/Treatment of Postoperative Effusion via Multi-Layer Suspension Technique

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600118317
Enrollment
Unknown
Registered
2026-02-04
Start date
2025-10-01
Completion date
Unknown
Last updated
2026-02-09

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

Conditions

Postoperative Effusion in PEEK Cranioplasty

Interventions

Single-layer Suspension Technique Group:NA
Multi-Layer Suspension Technique Group:NA

Sponsors

Chinese People's Liberation Army (PLA) Joint Logistics Support Force 960th Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
3 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Age > 3 years and = 1 month and <= 1 year.

Exclusion criteria

Exclusion criteria: 1.Skin at the defect site with infection, extensive scar tissue, or poor local blood supply; 2. Patients with obvious symptoms of intracranial hypertension; 3. Coagulation dysfunction; 4. Patients with poor compliance, who are expected to be unable to complete the surgical plan, treatment, imaging examinations, and follow-up in accordance with the study protocol; 5. Any other reasons deemed unsuitable for enrollment by the researchers.

Design outcomes

Primary

MeasureTime frame
Incidence Rate of Postoperative Effusion;Incidence Rate of Postoperative Epilepsy;Glasgow Coma Scale Score;Glasgow Outcome Scale Score;Modified Rankin Scale Score;

Secondary

MeasureTime frame
Incidence Rate of Postoperative Hydrocephalus;Incidence Rate of Postoperative Incisional Infection;Length of Hospital Stay;In-hospital Mortality Rate;

Countries

China

Contacts

Public ContactBodong Wang

Department of Neurosurgery, the 960th Hospital of PLA

hsq1157694103@163.com+86 185 7395 8790

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 15, 2026