Trial · NCT03530462
To Explore Cognitive Neural Mechanism of Autoimmune Encephalitis by Using Neuropsychological Tests and Multi-modal MRI
NCT03530462, Completed, First Affiliated Hospital of Zhejiang University
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. To Explore Cognitive Neural Mechanism of Autoimmune Encephalitis by Using Neuropsychological Tests and Multi-modal MRI. Trials, record NCT03530462. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT03530462
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- To Explore Cognitive Neural Mechanism of Autoimmune Encephalitis by Using Neuropsychological Tests and Multi-modal MRI
- NCT number
- NCT03530462
- Status
- Completed
- Enrollment
- 22 participants, actual
- Lead sponsor
- First Affiliated Hospital of Zhejiang University
- Conditions
- Cognitive Impairment, Autoimmune Encephalitis
- Interventions
- rituximab, cyclophosphamide, Steroids, Intravenous immunoglobulin
- First posted
- 2018-05-21
- Last updated
- 2018-05-21
Source ClinicalTrials.gov
Registered outcomes10
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | brain functional connectivity changes | a minimum of 6 months following initial discharge from hospital | The study uses multi-model fMRI to measure changes of functional connectivity across regions during recovery |
| Secondary | verbal episodic memory | a minimum of 6 months following initial discharge from hospital | Chinese auditory verbal learning test (CAVLT) |
| Secondary | non-verbal episodic memory | a minimum of 6 months following initial discharge from hospital | Aggie Figures Learning Test (AFLT) |
| Secondary | working memory | a minimum of 6 months following initial discharge from hospital | working memory test |
| Secondary | emotion-anxiety | a minimum of 6 months following initial discharge from hospital | self-rating anxiety scale (SAS),the \*total\* range (20-80 scores), anxiety state (the total score is equal or above 41) |
| Secondary | emotion-depression | a minimum of 6 months following initial discharge from hospital | self-rating depression scale (SDS), the \*total\* range (20-80 scores), depression state (the total score is equal or above 41) |
| Secondary | executive control | a minimum of 6 months following initial discharge from hospital | Stroop test |
| Secondary | information processing speed | a minimum of 6 months following initial discharge from hospital | symbol-digit modalities test (SDMT) |
| Secondary | visual-spatial ability | a minimum of 6 months following initial discharge from hospital | block design test |
| Secondary | semantic fluency test | a minimum of 6 months following initial discharge from hospital | vegetable and fruit, animal |
Source ClinicalTrials.gov
Outcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests5
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
| Test | Named as | Source |
|---|---|---|
| Block Copy Test | Secondary outcome | ConductCognition |
| Category Fluency | Secondary outcome | ConductCognition |
| Stroop Color-Word Test | Secondary outcome | ConductCognition |
| Symbol Coding | Secondary outcome | ConductCognition |
| Verbal Learning | Secondary outcome | ConductCognition |
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT03530462
GET https://conductscience.org/api/trials/v1/NCT03530462/registered