Status:
UNKNOWN
Effects of 800mg of Rhodiola Rosea in Attention in Adults With Attention-Deficit/Hyperactivity Disorder
Lead Sponsor:
Hospital de Clinicas de Porto Alegre
Conditions:
Attention Deficit Hyperactivity Disorder
Eligibility:
All Genders
18+ years
Phase:
PHASE4
Brief Summary
This study evaluates the use of Rhodiola rosea in the attention of adults with Attention Deficit/Hyperactivity Disorder (ADHD). Half of participants will receive Rhodiola rosea 800mg, while the other ...
Detailed Description
The evaluation of new therapies in adults with Attention Deficit/Hyperactivity Disorder (ADHD) may be clinically useful. Rhodiola rosea is an herbal medicine used for centuries in various medical cond...
Eligibility Criteria
Inclusion
- Fulfillment of Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition, (DSM-5) diagnostic criteria for ADHD in Adults
- Intelligence Quotient (IQ) above 70
- Eligibility to Rhodiola rosea
Exclusion
- clinical contraindication to Rhodiola rosea
- any unstable chronic illness without proper treatment (hypertension, heart, kidney or liver disease, etc)
- any significant neurological disease (delirium, dementia, epilepsy, AIDS, head trauma, multiple sclerosis, stroke, etc)
- unstable psychiatric comorbidities requiring immediate treatment (risk of suicide, current Substance Use Disorder, etc.)
- pregnant, nursing or absence of reliable contraception
- current use of nicotine (\<30 days)
- use of anticoagulants
- current use of any psychoactive drug (\<30 days)
- prior use of stimulants
- current or lifetime psychosis
- current or lifetime bipolar disorder
Key Trial Info
Start Date :
April 1 2016
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
March 1 2021
Estimated Enrollment :
60 Patients enrolled
Trial Details
Trial ID
NCT02737033
Start Date
April 1 2016
End Date
March 1 2021
Last Update
May 29 2019
Active Locations (1)
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1
Hospital de Clínicas de Porto Alegre
Porto Alegre, Rio Grande do Sul, Brazil, 90035-903