- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04362709
Study of Post-anesthesia Management in Patients Undergoing Neurosurgery
April 22, 2024 updated by: Yuming Peng, Beijing Tiantan Hospital
A Prospective Cohort Study of Post-anesthesia Management in Patients Undergoing Neurosurgery
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.
Study Overview
Status
Recruiting
Conditions
Study Type
Observational
Enrollment (Estimated)
10000
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Yuming Peng, M.D., Ph.D
- Phone Number: 8610-59976658
- Email: florapym766@163.com
Study Locations
-
-
-
Beijing, China, 100070
- Recruiting
- Beijing Tiantan Hospital
-
Contact:
- Yuming Peng, M.D., Ph.D
- Phone Number: 8610-59976658
- Email: florapym766@163.com
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Sampling Method
Probability Sample
Study Population
Patients expected to returned to post-anesthesia care unit(PACU) after neurosurgical treatment in Beijing Tiantan hospital.
Description
Inclusion Criteria:
- Patients received neurosurgery in Beijing Tiantan hospital.
Exclusion Criteria:
- Preoperative severe cognitive dysfunction ;
- Refused to sign informed consent.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
---|
Postoperative complications
|
No postoperative complications
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
The incidence of postoperative complications in neurosurgery.
Time Frame: 5±2 days
|
The incidence of postoperative complications was diagnosed by the corresponding assessment scale.Complications include nausea, vomiting, delirium, delayed recovery, intracranial hematoma,etc.
|
5±2 days
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Chair: Yuming Peng, M.D., Ph.D, Department of Anesthesiology, Beijing Tiantan Hospital
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
December 2, 2019
Primary Completion (Estimated)
November 22, 2024
Study Completion (Estimated)
November 22, 2024
Study Registration Dates
First Submitted
January 14, 2020
First Submitted That Met QC Criteria
April 22, 2020
First Posted (Actual)
April 27, 2020
Study Record Updates
Last Update Posted (Actual)
April 24, 2024
Last Update Submitted That Met QC Criteria
April 22, 2024
Last Verified
April 1, 2024
More Information
Terms related to this study
Other Study ID Numbers
- 2019-10
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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