- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05647525
The Etiology of New-onset Status Epilepticus
December 13, 2022 updated by: Jie Liu
Sichuan Academy of Medical Sciences - Sichuan Provincial People's Hospital
This study will help to identify the causes of new epilepsy and provide a basis for the development of a rational and standardized diagnosis and treatment plan to reduce the rate of disability and death.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Actual)
60
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Sichuan
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Chengdu, Sichuan, China
- Jie Liu
-
-
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
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
N/A
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Patients were selected strictly according to the inclusion and exclusion criteria from January 2021 to December 2022 at Sichuan Academy of Medical Sciences.
Inpatient NOSE patients at Sichuan Provincial People's Hospital
Description
Inclusion Criteria:
- Clinical diagnosis of Status Epilepticus
- Sign the informed consent form
Exclusion Criteria:
- Patients with previous epilepsy
- Missing information such as basic information and treatment history
- Long-term smoking, alcohol and drug abuse
- Pregnant and breastfeeding women
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 |
Intervention / Treatment |
|---|---|
|
status epilepticus with autoimmune encephalitis; status epilepticus without autoimmune encephalitis
To study the relationship between autoimmune-related antibody titres and prognosis during the six-month follow-up
|
We only follow up without intervention.
Other Names:
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Death
Time Frame: 2021-12--2022-12
|
2021-12--2022-12
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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)
January 1, 2021
Primary Completion (Actual)
August 30, 2022
Study Completion (Actual)
September 30, 2022
Study Registration Dates
First Submitted
December 4, 2022
First Submitted That Met QC Criteria
December 4, 2022
First Posted (Actual)
December 12, 2022
Study Record Updates
Last Update Posted (Estimate)
December 15, 2022
Last Update Submitted That Met QC Criteria
December 13, 2022
Last Verified
December 1, 2022
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Liujiessy
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Undecided
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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-
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-
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