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Clinical Trials/NCT04221256
NCT04221256WithdrawnPhase 1

Dose-finding Study of Selective Serotonin Reuptake Inhibitors to Enhance Neuroplasticity

Burke Medical Research Institute1 site in 1 countryStarted: March 11, 2020Last updated:
Conditions
Interventions
Drugs

Trial Snapshot

Phase
Phase 1
Status
Withdrawn
Sponsor
Locations
1
Primary Endpoint
Change in motor evoked potential amplitude

Study Overview

Brief Summary

The brain is able to change throughout life in response to learning, or injury, or to adapt to changes in the environment, which is known as neuroplasticity. Stroke survivors suffer disabling chronic motor impairments that have proven challenging to improve. Increasing neuroplasticity using selective serotonin reuptake inhibitors (SSRIs) is a promising approach to promote motor recovery in patients with stroke.

Detailed Description

The brain is able to change throughout life in response to learning, or injury, or to adapt to changes in the environment, which is known as neuroplasticity. Stroke survivors suffer disabling chronic motor impairments that have proven challenging to improve. Increasing neuroplasticity using selective serotonin reuptake inhibitors (SSRIs) is a promising approach to promote motor recovery in patients with stroke. Selective serotonin reuptake inhibitors (SSRIs) are currently widely used for treatment of depression, but they also have been shown to be able to enhance neuroplasticity. A single dose of SSRI has been shown to improve hand function in patients with chronic stroke. SSRIs also enhance neuroplasticity in healthy individuals, as shown using paired associative stimulation (PAS), a non-invasive method which causes the brain's excitability to change. However, the best dose of SSRI to increase neuroplasticity is not yet established.

The purpose of this study is to (1) find the effective dose of the SSRI escitalopram to modulate PAS-induced plasticity in patients with stroke and healthy individuals and (2) determine the variability of escitalopram's effect on PAS-induced plasticity between individuals. We measure neuroplasticity with PAS, which causes the brain's excitability to change. During PAS, you would receive electrical stimulation over your wrist and magnetic stimulation to their scalp (called transcranial magnetic stimulation, or TMS) to increase the excitability of the motor area of the brain. You will be asked to participate in a screening visit and 8 study visits separated by at least 1 week. At each study visit, you will be given a single dose of escitalopram (5, 10 or 20) or placebo, and we will measure your brain's change in excitability after PAS.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Crossover
Primary Purpose
Treatment
Masking
Triple (Participant, Investigator, Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Arms & Interventions

Administration of SSRI

Experimental

Participants will be administered either 5, 10 or 20mg of SSRI escitalopram prior to paired associative stimulation.

Intervention: Administration of SSRI escitalopram (Drug)

Administration of SSRI

Experimental

Participants will be administered either 5, 10 or 20mg of SSRI escitalopram prior to paired associative stimulation.

Intervention: Paired Associative stimulation (Behavioral)

Administration of Placebo

Placebo Comparator

Participants will be administered a placebo prior to paired associative stimulation

Intervention: Paired Associative stimulation (Behavioral)

Administration of Placebo

Placebo Comparator

Participants will be administered a placebo prior to paired associative stimulation

Intervention: Administration of Placebo (Drug)

Outcomes

Primary Outcomes

Change in motor evoked potential amplitude

Time Frame: Baseline, Up to 30 minutes Post PAS

Assessment of corticospinal excitability

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Burke Medical Research Institute
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Tomoko Kitago

Lab Director Human Motor Recovery Laboratory Assistant Professor

Burke Medical Research Institute

Study Sites (1)

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