comparison of piezosurgery and conventional instruments in cranioplasty

Phase 4

• Conditions: Q75.0; Craniosynostosis

• Registration Number: DRKS00010553
• Lead Sponsor: Kinderneurochirurgie Asklepios Kinderklinik

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Completion: 2016-05-22
• Study Start: 2016-06-08
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 34

Inclusion Criteria

patients with craniosynostosis (trigonocephalus, plagiocephalus, brachycephalus, syndromale craniosynostosis) and indication for frontooribital Advancement

Exclusion Criteria

congenital heart defect, bleeding diathesis, systemic bone diseases

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
surgery time, complete blood count and amount of blood transfusion, soft tissue tears, edema, pain and bone healing are documented. The data evaluation is finished with the last parameters 4 - 6 month after cranioplasty (at the time of plate removal): the appraisal of ossification

Secondary Outcome Measures

Name	Time	Method
Postoperatively, the volume of blood losses through surgical hemoglobin measured three times during the first 5 days after surgery and a pain score is evaluated