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Completed

NCT Number: NCT01940978

A Study of Combination Therapy in Children With ADHD

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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Key information

Age range

6 year–12 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

SMRI (Schuster Medical Research Institute)

Van Nuys, California, 91403, United States

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • The subject and subject's parents speak English
  • Child or adolescent patients, male or female outpatients, who are at least 6 years of age, but must not yet have reached their 13th birthday prior to Visit 1, when informed consent is obtained
  • Patients must meet Diagnostic and Statistical Manual of Mental Disorders Fourth Edition (DSM-IV) diagnostic criteria for ADHD (any subtype) and score at least 1.5 standard deviations above the age norm for their diagnostic subtype using published norms for the Swanson, Nolan and Pelham Questionnaire: Attention-Deficit/Hyperactivity Disorder Subscale (SNAP-IV ADHD Subscale) score at both Visit 1 and 2
  • Laboratory results, including serum chemistries, hematology, and urinalysis, must show no clinically significant abnormalities (clinically significant is defined as laboratory values requiring acute medical intervention, indicating a serious medical illness, or requiring further medical evaluation in the judgment of the investigator)
  • Patients and parents have been judged by the investigator to be reliable to keep appointments for clinic visits and all tests, including venipuncture, and examinations required by the protocol.
  • Patient has not been on stimulants for at least 2 weeks.

Exclusion criteria

  • Patients who have a documented history of Bipolar I or II disorder, or any history of psychosis. Diabetic patients or patients on chronic steroids.
  • Patients with a history of any seizure disorder (other than febrile seizures) or patients who have taken (or are currently taking) anticonvulsants for seizure control are not eligible to participate
  • Patients at serious suicidal risk as defined by 1) suicidal ideation as endorsed on items 4 and 5 of the C-SSRS within the past year, 2) suicidal behaviors detected by the C-SSRS during the past two years; or 3) psychiatric interview and examination
  • Patients with significant cardiovascular disease or other conditions that could be aggravated by an increased heart rate or increased blood pressure
  • Patients who have any medical condition that would increase sympathetic nervous system activity markedly (for example, catecholamine-secreting neural tumor), or who are taking a medication on a daily basis (for example, albuterol, inhalation aerosols, pseudoephedrine), that has sympathomimetic activity. Such medications can be taken on an as-needed basis
  • Presence of contraindications for methylphenidate or cyproheptadine hydrochloride
  • Patients who have had prior serious adverse reaction to stimulants.
  • Parental or (immediate) family history of substance abuse

Treatment and study plan

Methylphenidate ER

Drug

Watson generic, starting dose 18mg QD

Other names: Concerta

Cyproheptadine

Drug

cyproheptadine hydrochloride

Other names: Periactin

Primary outcomes

  1. Appetite - Appetite and Dietary Assessment Tool (ADAT) developed by Burrowes et al (1996)

    Time frame: 0, 12 weeks

Secondary outcomes

  1. Swanson, Nolan & Pelham Rating Scale - Revised (SNAP-IV): ADHD Combined Score

    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).

  2. Weight

    Time frame: 0,1,5,9,12 Weeks

  3. Appetite - VAS - Visual Analogue Scale

    Time frame: 0,1,5,9,12

  4. Clinical Global Impressions - Improvement(CGI-I): ADHD Score

    Time frame: 1,5,9,12 weeks

  5. Clinical Global Impressions - Severity(CGI-S): ADHD Score

    Time frame: 0,1,5,9,12

  6. Clinical Global Impressions - Effectiveness(CGI-E): ADHD Score

    Time frame: 1,5,9,12

  7. Appetite - Appetite and Dietary Assessment Tool (ADAT) developed by Burrowes et al (1996)

    Time frame: 1,5,9 weeks

Sponsors and collaborators

Lead sponsor

Douglas Sears

Indiv

Registry information

Official study title

A Double-Blind Placebo-Controlled Study of Combination Therapy in Children With ADHD

Important dates

Study start
2014
Primary completion
2015
Study completion
2015
First posted
Sep 12, 2013
Registry last updated
Apr 10, 2015

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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