NCT04362709

Brief 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. 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.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
10,000

participants targeted

Target at P75+ for all trials

Timeline
31mo left

Started Dec 2019

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress72%
Dec 2019Nov 2028

Study Start

First participant enrolled

December 2, 2019

Completed
1 month until next milestone

First Submitted

Initial submission to the registry

January 14, 2020

Completed
3 months until next milestone

First Posted

Study publicly available on registry

April 27, 2020

Completed
8.6 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 22, 2028

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

November 22, 2028

Last Updated

July 18, 2025

Status Verified

July 1, 2025

Enrollment Period

9 years

First QC Date

January 14, 2020

Last Update Submit

July 17, 2025

Conditions

AnesthesiaNeurosurgeryComplication

Outcome Measures

Primary Outcomes (1)

  • 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.

    5±2 days

Study Arms (2)

Postoperative complications

No postoperative complications

Eligibility Criteria

Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

Patients expected to returned to post-anesthesia care unit(PACU) after neurosurgical treatment in Beijing Tiantan hospital.

You may qualify if:

  • Patients received neurosurgery in Beijing Tiantan hospital.

You may not qualify if:

  • Preoperative severe cognitive dysfunction ；
  • Refused to sign informed consent.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Beijing TianTan Hospital

Beijing, 100070, China

RECRUITING

Study Officials

  • Yuming Peng, M.D., Ph.D

    Department of Anesthesiology, Beijing Tiantan Hospital

    STUDY CHAIR

Central Study Contacts

Yuming Peng, M.D., Ph.D

CONTACT

8610-59976658florapym766@163.com

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Target Duration
3 Years
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Associate professor

Study Record Dates

First Submitted

January 14, 2020

First Posted

April 27, 2020

Study Start

December 2, 2019

Primary Completion (Estimated)

November 22, 2028

Study Completion (Estimated)

November 22, 2028

Last Updated

July 18, 2025

Record last verified: 2025-07

Locations

CN(1)