SMRI (Schuster Medical Research Institute)
Van Nuys, California, 91403, United States
NCT Number: NCT01940978
Lack of appetite and weight loss are a common side effect of ADHD therapy with amphetamines such as methylphenidate. Lack of sufficient food intake has been shown to have negative effects on weight and height as well as learning and memory.
There is no current treatment to prevent this loss of appetite except discontinuation or reduction of the methylphenidate. Discontinuation or reduction of the drug can cause the return of ADHD symptoms.
The purpose of this study is to compare the effects, good and/or bad, of two doses of a drug, cyproheptadine, vs placebo to find out if cyproheptadine prevents the appetite suppression associated with methylphenidate.
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Notify Me6 year–12 year
All sexes
Interventional
Phase 4
Van Nuys, California, 91403, United States
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Watson generic, starting dose 18mg QD
Other names: Concerta
cyproheptadine hydrochloride
Other names: Periactin
Time frame: 0, 12 weeks
Time frame: 0,1,5,9,12 weeks
The items from the DSM-IV (1994) criteria for Attention-Deficit/Hyperactivity Disorder (ADHD) are included for the two subsets of symptoms: inattention (items #1-#9) and hyperactivity/ impulsivity (items #11-#19).
Time frame: 0,1,5,9,12 Weeks
Time frame: 0,1,5,9,12
Time frame: 1,5,9,12 weeks
Time frame: 0,1,5,9,12
Time frame: 1,5,9,12
Time frame: 1,5,9 weeks
Douglas Sears
Indiv
A Double-Blind Placebo-Controlled Study of Combination Therapy in Children With ADHD
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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