NL-OMON31400
Recruiting
Not Applicable
The relationship between clinical efficacy and efficacy as measured by two versions of the Continuous Performance Test of OROS-Methylphenidate in adults with ADHD: a double blind placebo controlled medication trial. - CPT and OROS-Mph in adults with ADHD
Parnassia (Den Haag)0 sites44 target enrollmentTBD
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- ADHD
- Sponsor
- Parnassia (Den Haag)
- Enrollment
- 44
- Status
- Recruiting
- Last Updated
- last year
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •ADHD\-combined subtype has been diagnosed according to regular clinical diagnostic procedures
- •Patient is able to read and understand Patient Information
- •Patient has signed Informed Consent Form
- •Patient is able and willing to fill out questionnaires
- •Patient is able and willing to meet follow up appointments for the study
Exclusion Criteria
- •\- Comorbid disorder (Axis I) that is very severe at intake and that may interfere with need of rapid treatment or with the goals of the study:
- •Severe current substance abuse or substance dependence (alcohol: more than 2 consumptions per day or for women more than 15 consumptions in total per week or for men more than 21 conusmptions in total per week. Cannabis: more than one joint per day. Hard drugs: exclusion per se);Anxiety and/or mood disorders will be treated with SSRIs before treatment for ADHD starts.;\- Use of the following medications within a month prior to participation to the study: stimulants, anti\-psychotic medication, clonidine, benzodiazepines, beta\-blockers;\- Symptoms of dementia, amnestic disorders or other cognitive disorders;\- Symptoms of serious Cluster B Axis II psychopathology that may interfere with cooperation to the study;\- For women: pregnancy, breastfeeding of lack of suitable contraception;\- Mental retardation;\- Insufficient fluency in the Dutch language
Outcomes
Primary Outcomes
Not specified
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