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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04362709
Other study ID # 2019-10
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date December 2, 2019
Est. completion date November 22, 2024

Study information

Verified date April 2024
Source Beijing Tiantan Hospital
Contact Yuming Peng, M.D., Ph.D
Phone 8610-59976658
Email florapym766@163.com
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical 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. 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.


Recruitment information / eligibility

Status Recruiting
Enrollment 10000
Est. completion date November 22, 2024
Est. primary completion date November 22, 2024
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - Patients received neurosurgery in Beijing Tiantan hospital. Exclusion Criteria: - Preoperative severe cognitive dysfunction ; - Refused to sign informed consent.

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
China Beijing TianTan Hospital Beijing

Sponsors (1)

Lead Sponsor Collaborator
Beijing Tiantan Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary 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
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