Study of Post-anesthesia Management in Patients Undergoing Neurosurgery
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- This is an observational study: the protocol does not assign a study treatment.
- Who it may be relevant to
- Registry conditions: Anesthesia, Neurosurgery, Complication. Basic parameters: No limits · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- China
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
A Prospective Cohort Study of Post-anesthesia Management in Patients Undergoing Neurosurgery
Overview
The postoperative complications of neurosurgery are various and complex, which brings heavy economic and social burden to families. Timely detection and early intervention can help reduce the incidence of adverse events and mortality. The main purpose of this study is to analyze the possible factors related to postoperative complications of Neurosurgery, so as to achieve the prospective prevention and treatment of postoperative complications of neurosurgery.
Primary outcome measures
- The incidence of postoperative complications in neurosurgery. [Time frame: 5±2 days]
Eligibility criteria
Inclusion criteria
- Patients received neurosurgery in Beijing Tiantan hospital.
Exclusion criteria
- Preoperative severe cognitive dysfunction ;
- Refused to sign informed consent.
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Observational model
- Cohort
Study locations
China · 1 center
- Beijing TianTan Hospital — Beijing
Identifiers
NCT: NCT04362709 · 2019-10