AnesthesiaNCT04362709
Study of Post-anesthesia Management in Patients Undergoing Neurosurgery
An observational study of Anesthesia and Neurosurgery, run by Beijing Tiantan Hospital at 1 site in China.
Trial summary
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. Read more about this study
- Who is it for?
- Any age
- Conditions the study is for
- Anesthesia, Neurosurgery, Complication
- How many people
- 10,000 participants
- Where
- 1 siteChina
- Study dates
- 2 Dec 2019to 22 Nov 2028
- How long will I take part?
- 3 Years
- Phase
- Observational
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages Any age
- All sexes
- No healthy volunteers
- Child, Adult, Older adult
Study population: Patients expected to returned to post-anesthesia care unit(PACU) after neurosurgical treatment in Beijing Tiantan hospital.
Who may be able to join
- Patients received neurosurgery in Beijing Tiantan hospital.
Who cannot join
- Preoperative severe cognitive dysfunction ；
- Refused to sign informed consent.
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
China1 site, 1 recruiting
- Recruiting
Beijing TianTan Hospital
Beijing, 100070
Yuming Peng, M.D., Ph.D, 8610-59976658, florapym766@163.com
About this study
Official title: 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.
- Conditions
- Anesthesia, Neurosurgery, Complication
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
| Study group | Role | What they receive |
|---|---|---|
| Postoperative complications | Not described | |
| No postoperative complications | Not described |
What is being measured
The primary outcome is the main question the study is designed to answer.
The incidence of postoperative complications in neurosurgery.
The incidence of postoperative complications was diagnosed by the corresponding assessment scale.Complications include nausea, vomiting, delirium, delayed recovery, intracranial hematoma,etc.
Measured: 5±2 days
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted27 Apr 2020
- Study start2 Dec 2019
- Primary completion22 Nov 2028 (estimated)
- Study completion22 Nov 2028 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for AnesthesiaStudies of the same condition, open and under way.
- More trials run by Beijing Tiantan HospitalThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 10,000 participants (estimated)
- Target duration
- 3 Years
Sponsor and investigators
- Lead sponsor
- Beijing Tiantan Hospital
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Yuming Peng, Beijing Tiantan Hospital
- Investigators
- Yuming Peng, M.D., Ph.D, Study chair, Department of Anesthesiology, Beijing Tiantan Hospital
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT04362709
- Sponsor's protocol ID
- 2019-10
- Status last verified
- Jul 2025
- First submitted
- 14 Jan 2020
- Last updated
- 18 Jul 2025
- Results posted
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 18 Jul 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Prospective Cohort Study of Post-anesthesia Management in Patients Undergoing Neurosurgery
- ClinicalTrials.gov ID
- NCT04362709
- Acronym / sponsor ID
- 2019-10
- Conditions
- Anesthesia, Neurosurgery, Complication
- Study type
- Observational
- Recruitment status
- Recruiting
- Enrolment
- 10,000 participants (estimated)
- Lead sponsor
- Beijing Tiantan HospitalUniversity, hospital or other
- Study start
- 2 Dec 2019 (actual)
- Primary completion
- 22 Nov 2028 (estimated)
- Study completion
- 22 Nov 2028 (estimated)
- First posted
- 27 Apr 2020 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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 design
- Observational model
- Cohort
- Time perspective
- Prospective
- Target follow-up
- 3 Years
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Postoperative complications | – | – |
| No postoperative complications | – | – |
Who may qualify
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child, Adult, Older adult
- Study population
- Patients expected to returned to post-anesthesia care unit(PACU) after neurosurgical treatment in Beijing Tiantan hospital.
Key inclusion criteria (1 listed)
- Patients received neurosurgery in Beijing Tiantan hospital.
Key exclusion criteria (2 listed)
- Preoperative severe cognitive dysfunction ；
- Refused to sign informed consent.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
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.
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 18 Jul 2025.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Yuming Peng, M.D., Ph.D study chair
Department of Anesthesiology, Beijing Tiantan Hospital
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Anesthesia and Neurosurgery, run by Beijing Tiantan Hospital at 1 site in China.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 1 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: looking for participants now, as of the sponsor's last update on 18 Jul 2025. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in China. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Yuming Peng, M.D., Ph.D (8610-59976658, florapym766@163.com), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
The incidence of postoperative complications in neurosurgery. (time frame: 5±2 days). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 18 Jul 2025.