Ignite Creation Date:
2025-12-24 @ 7:58 PM
Ignite Modification Date:
2025-12-25 @ 5:32 PM
Study NCT ID:
NCT04791904
Status:
COMPLETED
Last Update Posted:
2022-08-24
First Post:
2021-03-06
Is NOT Gene Therapy:
False
Has Adverse Events:
False
Brief Title:
Predictive Factors for Cranioplasty Complications - A Decade Experience
Sponsor:
Universidade do Porto
Organization:
Study Overview
Official Title:
Predictive Factors for Cranioplasty Complications - A Decade Experience
Status:
COMPLETED
Status Verified Date:
2022-08
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
This is a single-center, observational retrospective study. This study aims to identify predictive factors of complications for patients submitted to cranioplasty after decompressive craniectomy for all types of etiologies.
All patients submitted to cranioplasty since 2008 will be analyzed.
All patients submitted to cranioplasty since 2008 will be analyzed.
Detailed Description:
Patients submitted to cranioplasty since 2008 to 2019 will be retrospectively analyzed.
Will be considered for analysis all cases treated after decompressive craniectomy. Will be excluded patients with incomplete clinical or imaging records.
Main factors determined as a possible influence on complications after cranioplasty will be recorded focusing on patients characteristics, craniectomy characteristics, surgical timing, and cranioplasty materials.
Patients' records will be review by two investigators and data will be verified by a third investigator. records will be anonymously recorded.
Will be considered for analysis all cases treated after decompressive craniectomy. Will be excluded patients with incomplete clinical or imaging records.
Main factors determined as a possible influence on complications after cranioplasty will be recorded focusing on patients characteristics, craniectomy characteristics, surgical timing, and cranioplasty materials.
Patients' records will be review by two investigators and data will be verified by a third investigator. records will be anonymously recorded.
Study Oversight
Has Oversight DMC:
False
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?: