Clinical trial · Observational
Re-craniotomy and Complications After Elective Neurosurgery
Predictive Factors of Re-craniotomy and Major Non-neurological Complications in Elective Neurosurgery: A Prospective Cohort Study
NCT03910556CI-TRIAL-00038098completedClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
This study is a prospective cohort study to find the incidence of re-craniotomy and predictive factors. The secondary outcomes are to find the incidence of major non-neurological complications and predictive factors.
Conditions
Conditions (4)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Brain Cancer | Malignant Brain Neoplasm | ALIAS | 0.90 |
| Brain Metastases | — | UNRESOLVED | — |
| Brain Neoplasms | Brain Neoplasm | ONTOLOGY_EXACT | 0.90 |
| Brain Tumor | Brain Neoplasm | ALIAS | 0.90 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Propofol | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- label
- no complication
- description
- the patients who did not develop any kind of complication and no re-craniotomy
- interventionNames
- Drug: Propofol
- label
- with complication (s)
- description
- the patients who developed at least one of non-neurological complication or required re-craniotomy
- interventionNames
- Drug: Propofol
Primary outcomes (2)
- measure
- re-craniotomy
- timeFrame
- the first 24 hours
- description
- number of participants who required re-craniotomy assessed by the neurosurgeon
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 75 Years
Show eligibility criteria text
Inclusion Criteria: * Patients who are scheduled for elective craniotomy during 2017-2019 * Patients who are planned for general anesthesia * Patients have read the study information and signed in the consent form Exclusion Criteria: * Patients who are unable to understand and sign in the consent form * Patients who are scheduled for minor surgical procedures such as ventriculostomy and VP-shunt
References
Publications (0)
Data not yet available
No reference posted for this study.