Analyzing post-anesthesia management in neurosurgery patients
A Prospective Cohort Study of Post-anesthesia Management in Patients Undergoing Neurosurgery
This study looks at patients who have had brain surgery to see what factors might lead to complications after anesthesia, hoping to improve their recovery and safety.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 10000 (estimated) |
| Sex | All |
| Sponsor | Beijing Tiantan Hospital Academic / other |
| Locations | 1 site (Beijing) |
| Trial ID | NCT04362709 on ClinicalTrials.gov |
What this trial studies
This observational study focuses on patients who have undergone neurosurgery at Beijing Tiantan Hospital. It aims to identify factors associated with postoperative complications to facilitate timely detection and intervention. By analyzing these factors, the study seeks to improve outcomes and reduce the incidence of adverse events and mortality in neurosurgery patients. The findings could lead to better management strategies for post-anesthesia care in this population.
Who should consider this trial
Good fit: Ideal candidates for this study are patients who have recently undergone neurosurgery at Beijing Tiantan Hospital.
Not a fit: Patients with severe cognitive dysfunction prior to surgery or those who refuse to sign informed consent may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could significantly reduce postoperative complications and improve recovery outcomes for neurosurgery patients.
How similar studies have performed: While similar observational studies have been conducted, this specific focus on postoperative management in neurosurgery is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patients received neurosurgery in Beijing Tiantan hospital. Exclusion Criteria: * Preoperative severe cognitive dysfunction ； * Refused to sign informed consent.
Where this trial is running
Beijing
- Beijing TianTan Hospital — Beijing, China (Recruiting)
Study contacts
- Study coordinator: Yuming Peng, M.D., Ph.D
- Email: florapym766@163.com
- Phone: 8610-59976658
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.