Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
NA
90 participants
INTERVENTIONAL
2020-10-10
2022-03-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
BASIC_SCIENCE
DOUBLE
Study Groups
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Losartan group
Losartan
administration of losartan (50 mg) (oral)
Placebo group
Placebo Oral Tablet
administration of placebo (oral)
Interventions
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Losartan
administration of losartan (50 mg) (oral)
Placebo Oral Tablet
administration of placebo (oral)
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* medical or psychiatric illness
* hypertension
18 Years
30 Years
ALL
Yes
Sponsors
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University of Electronic Science and Technology of China
OTHER
Responsible Party
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Benjamin Becker
Professor
Principal Investigators
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Benjamin Becker, PhD
Role: PRINCIPAL_INVESTIGATOR
University of Electronic Science and Technology of China
Locations
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University of Electronic Science and Technology of China
Chengdu, Sichuan, China
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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UESTC-neuSCAN-73
Identifier Type: -
Identifier Source: org_study_id