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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03530462
Other study ID # multi-mode MRIs- encephalitis
Secondary ID
Status Completed
Phase
First received
Last updated
Start date April 7, 2017
Est. completion date February 28, 2018

Study information

Verified date February 2018
Source First Affiliated Hospital of Zhejiang University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Most of patients with autoimmune encephalitis are left with permanent cognitive deficits of varying severity. The patients' life and career would be affected definitely by cognitive deficits. Recently, more and more clinical physician have begun to focus on cognitive impairment of patients with autoimmune encephalitis. Generally, the outcome was measured by the modified Rankin Scale (mRS). However, the mRS are commonly used to evaluate the degree of disability or dependence in the daily activities of the patients suffering from a stroke and cognition function were minimally evaluated in this scale. It is crucial to adopt detailed cognition tools to study the long-term cognitive outcomes and as an indicator of overall curative effect judgment in autoimmune encephalitis.

Currently, only early immunotherapy is uniformly and consistently considered to produce favorable cognitive outcomes. However, studies concerning the association of second-line immunotherapy with cognitive outcomes have been scarce and have shown conflicting results regarding autoimmune encephalitis.

Hence, the goal of this study was to explore cognitive neural mechanism of autoimmune encephalitis by using neuropsychological tests and multi-mode MRIs.


Description:

The goal of this study was to explore cognitive neural mechanism of different types of autoimmune encephalitis by using neuropsychological tests and multi-mode MRIs. Neuropsychological tests involves the assessments of different cognitive domains. And multi-mode MRIs contains resting-fMRI, DTI and task-related fMRI.


Recruitment information / eligibility

Status Completed
Enrollment 22
Est. completion date February 28, 2018
Est. primary completion date February 28, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 16 Years to 60 Years
Eligibility Inclusion Criteria: Diagnosis was established in all patients based on characteristic clinical presentation and detection of immunoglobulin G (IgG) antibodies.

Exclusion Criteria:

1. age >60 years or <16 years

2. notable lesions, such as tumors, scars, or vascular malformations, on brain MRI

3. a history of other neuropsychiatric disorders. -

Study Design


Intervention

Drug:
rituximab
375 mg/m2 weekly for 4 weeks
cyclophosphamide
750 mg/m2 monthly for 4-6 cycles depending on the response
Steroids
500-1000 mg of methylprednisolone daily for 3 days, then tapered doses
Intravenous immunoglobulin
intravenous immunoglobulin (IVIG) with or without plasmapheresis

Locations

Country Name City State
China The First Affiliated Hospital, Zhejiang University Hangzhou Zhejiang

Sponsors (1)

Lead Sponsor Collaborator
First Affiliated Hospital of Zhejiang University

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary brain functional connectivity changes The study uses multi-model fMRI to measure changes of functional connectivity across regions during recovery a minimum of 6 months following initial discharge from hospital
Secondary verbal episodic memory Chinese auditory verbal learning test (CAVLT) a minimum of 6 months following initial discharge from hospital
Secondary non-verbal episodic memory Aggie Figures Learning Test (AFLT) a minimum of 6 months following initial discharge from hospital
Secondary working memory working memory test a minimum of 6 months following initial discharge from hospital
Secondary emotion-anxiety self-rating anxiety scale (SAS),the *total* range (20-80 scores), anxiety state (the total score is equal or above 41) a minimum of 6 months following initial discharge from hospital
Secondary emotion-depression self-rating depression scale (SDS), the *total* range (20-80 scores), depression state (the total score is equal or above 41) a minimum of 6 months following initial discharge from hospital
Secondary executive control Stroop test a minimum of 6 months following initial discharge from hospital
Secondary information processing speed symbol-digit modalities test (SDMT) a minimum of 6 months following initial discharge from hospital
Secondary visual-spatial ability block design test a minimum of 6 months following initial discharge from hospital
Secondary semantic fluency test vegetable and fruit, animal a minimum of 6 months following initial discharge from hospital
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