Table of contents
- Trial overview
- Who participates
- What is being studied
- Main outcomes
- Study design and phase
- Trial status and size
Trial overview
The main trial in the source data is a randomized crossover clinical trial that compares Lisdexamfetamine Dimesylate with methylphenidate in pediatric patients with ADHD and type 1 diabetes.[1] The study title says it is looking at two pharmacological therapies and includes both lisdexamphetamine and methylphenidate in children with these two conditions.[1]
Who participates
The trial is designed for pediatric patients, which means children and adolescents.[1] The brief summary says the study population has ADHD and type 1 diabetes.[1]
What is being studied
The study is comparing Lisdexamfetamine Dimesylate with methylphenidate, which is another medicine used in the trial.[1] The goal is to see how each treatment affects ADHD symptoms over time in children and adolescents who also have type 1 diabetes.[1]
The trial uses the names LDX for lisdexamphetamine and MPH for methylphenidate in the outcome description.[1] The study also includes a period before drug treatment, after completion of PTBM, and then compares symptom scores after 6 months of pharmacotherapy.[1]
Main outcomes
The main outcome is the change in ADHD symptom scores on the Conners 3 questionnaire.[1] The trial looks at two parts of the scale: inattention and hyperactivity/impulsivity.[1]
Researchers compare the score before pharmacotherapy with the score after 6 months of treatment for Lisdexamfetamine Dimesylate or methylphenidate.[1] They also assess the same change for the other drug, with the endpoint evaluated by an investigator who is blinded to patient allocation.[1]
Another main endpoint is the number and frequency of adverse events, which are unwanted medical problems reported during the study.[1] These events are described using the MedDRA dictionary, a standard way to record medical terms in research.[1]
Study design and phase
The study is listed as interventional, which means participants receive a treatment as part of the research.[1] It is a Phase 2 trial, so it is focused on learning more about treatment effects and safety in a specific group of patients.[1]
The crossover design means participants are expected to receive more than one treatment during the study, allowing researchers to compare the medicines within the same patient group.[1]
Trial status and size
The trial status is Authorised.[1] The planned enrollment is 150 participants.[1]
The source data do not give more details about results, so this article focuses on the study plan, the target population, and the outcomes being measured.[1]



