A Registration Study on Depression in Patients With Epilepsy
A Registration Study on Drug Treatment for Comorbid Depression in Patients With Epilepsy in East China
1 other identifier
observational
320
1 country
7
Brief Summary
The aim of this study is to register the drug treatment of depression in patients with epilepsy in East China.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Feb 2018
Longer than P75 for all trials
7 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
August 3, 2017
CompletedFirst Posted
Study publicly available on registry
August 14, 2017
CompletedStudy Start
First participant enrolled
February 1, 2018
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 31, 2021
CompletedStudy Completion
Last participant's last visit for all outcomes
January 31, 2022
CompletedJanuary 11, 2022
December 1, 2021
3.9 years
August 3, 2017
December 19, 2021
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
the drug treatment rate of depression in patients with epilepsy
the drug treatment rate at baseline and 6 months at follow-up
6 months
Secondary Outcomes (1)
the influence of depression on seizure-control
6 months
Study Arms (1)
patients with the comorbidity of epilepsy and depression
the clinical data, psychological assessment, and drug treatments will be investigated in patients with the comorbidity of epilepsy and depression
Eligibility Criteria
patients with the comorbidity of epilepsy and depression present to the neurology department at 8 tertiary hospitals in East China
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (7)
Department of Neurology, Huashan Hospital, Fudan University, Shanghai, China
Shanghai, Shanghai Municipality, 200040, China
Department of Neurology, Second Affiliated Hospital of Zhejiang University School of Medicine
Hangzhou, Zhejiang, 310009, China
Anhui Provincial Hospital
Hefei, China
Nanjing Brain Hospital
Nanjing, China
Shanghai General Hospital
Shanghai, China
The Second Affiliated Hospital of Suzhou University
Suzhou, China
The First Affiliated Hospital of Wenzhou Medical University
Wenzhou, China
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Xin Wang, PhD
Fudan University
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Target Duration
- 6 Months
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
August 3, 2017
First Posted
August 14, 2017
Study Start
February 1, 2018
Primary Completion
December 31, 2021
Study Completion
January 31, 2022
Last Updated
January 11, 2022
Record last verified: 2021-12