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Status unknownNCT04606212Updated Oct 28, 2020

The Effects of Losartan on Emotion Processing

An interventional study of Losartan and Placebo Oral Tablet in Healthy, sponsored by University of Electronic Science and Technology of China. Status unknown at 1 site in China. Open to participants aged 18 Years to 30 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2020-10-28.

Sponsored by University of Electronic Science and Technology of China · Not applicable, Interventional, and Basic science

The sponsor has not verified this record recently (last verified Oct 2020), so the status shown — last known as Recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
90
Allocation
Randomized
Ages
18 Years to 30 Years
Sex
All
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Study summary

The aim of the study is to investigate the effect of losartan (50mg, single dose) on salience processing

Read the detailed description

In a double-blind, between-subject, placebo-controlled design the effects of a single dose of losartan (50mg) on salience processing in healthy participants will be examined. The study will adopt a previously validated visual Oddball fMRI paradigm, starting 90 minutes after subjects receive 50mg losartan or placebo. The task requires participants to respond to emotional and novelty oddballs. Neural activity will be assessed by the acquisition of functional magnetic resonance imaging (fMRI) data.

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Conditions studied

  • Healthy

Keywords

  • Losartan
  • emotion processing
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In context

Lead sponsor

University of Electronic Science and Technology of China is the lead sponsor of 109 studies on the registry; 35 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years to 30 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Healthy subjects without past or current psychiatric or neurological disorders

Exclusion criteria

Exclusion Criteria:

  • history of head injury
  • medical or psychiatric illness
  • hypertension
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Study design

Phase
Not applicable
Primary purpose
Basic science
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Investigator)
Enrollment
90 participants (estimated)

Study arms

  • Experimental
    Losartan group

    Drug: Losartan

  • Placebo comparator
    Placebo group

    Drug: Placebo Oral Tablet

Interventions

  • DrugLosartan

    administration of losartan (50 mg) (oral)

  • DrugPlacebo Oral Tablet

    administration of placebo (oral)

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What researchers measure

Primary outcomes

  1. Neural activity as measured by BOLD fMRI during processing of emotional and novel stimuli

    During the oddball paradigm a series of pictures will be presented in rapid succession. Some of the stimuli are oddballs, with respect to emotional content (highly threatening stimuli) or novelty (novel stimuli). Neural activity will be measured by functional magnetic resonance imaging (fMRI). The fMRI data will be examined using a Generalized Linear Model approach. The analysis will examine neural activity in terms of the blood oxygenation dependent (BOLD) response towards threatening and novel oddballs. Effects of treatment on the BOLD response towards threatening and novel oddballs will be examined by comparing the losartan- and placebo-treated subjects.

    Time frame: 105 to 145 minutes after treatment administration

Secondary outcomes

  1. Neural activity as measured by BOLD fMRI during processing of different categories of emotional and novel stimuli

    The oddball paradigm will include different stimulus categories (animal pictures and human faces). Each category will include oddballs, with respect to emotional content (highly threatening stimuli) or novelty (novel stimuli). Neural activity will be measured by functional magnetic resonance imaging (fMRI). The fMRI data will be examined using a Generalized Linear Model approach. The analysis will examine neural activity differences between the stimulus categories (animal pictures, human face pictures) in terms of the blood oxygenation dependent (BOLD) response. Effects of treatment on the BOLD response towards different stimulus categories will be examined by comparing the losartan- and placebo-treated subjects.

    Time frame: 105 to 145 minutes after treatment administration

  2. Accuracy for target oddballs

    Before the paradigm two stimuli will be designated as 'target' and subjects are required to respond by button press to this target. The accuracy for target detection will be computed. Effects of treatment will be examined by comparing the losartan- and placebo-treated subjects.

    Time frame: 105 to 145 minutes after treatment administration

  3. Reaction times for target oddballs

    Before the paradigm two stimuli will be designated as 'target' and subjects are required to respond by button press to this target. The reaction times for correctly identified targets will be computed. Effects of treatment will be examined by comparing reaction times between the losartan- and placebo-treated subjects.

    Time frame: 105 to 145 minutes after treatment administration

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Study locations

1 of 1 sites recruiting
  • University of Electronic Science and Technology of China
    Chengdu, Sichuan 611731, China
    Recruiting
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References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 28, 2020, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT04606212
Lead sponsor
University of Electronic Science and Technology of China
Responsible party
Benjamin Becker (Professor, University of Electronic Science and Technology of China) — Principal investigator
First posted
Oct 28, 2020
Start date
Oct 10, 2020
Primary completion
Dec 31, 2021 (estimated)
Completion
Mar 31, 2022 (estimated)
Last update
Oct 28, 2020

Study contacts

Weihua Zhao, PhD
Contact
zarazhao.uestc@outlook.com
86-28-61830811
Benjamin Becker, PhD
principal investigator · University of Electronic Science and Technology of China

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Oct 2020. You cannot join it, but the record below documents what was studied.

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