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Clinical Trials/NCT04903353
NCT04903353CompletedPhase 4

Pragmatic Trial Comparing Weight Gain in Children With Autism Taking Risperidone Versus Aripiprazole

Vanderbilt University Medical Center1 site in 1 country30 target enrollmentStarted: February 1, 2022Last updated:
Conditions
Interventions
Drugs

Trial Snapshot

Phase
Phase 4
Status
Completed
Enrollment
30
Locations
1
Primary Endpoint
weight gain

Study Overview

Brief Summary

This study aims to compare two FDA approved medications (aripiprazole and risperidone) for the treatment of behavioral dysregulation in children with autism spectrum disorders. This trial, done in the context of routine clinical care, will seek to evaluate whether aripiprazole or risperidone is associated with more weight gain in children.

Detailed Description

Autism is a developmental disability with increasing prevalence in our society. Currently one out of fifty-nine children in the United States has this condition. Many children with autism experience behavioral dysregulation such as irritability and aggression.

Currently, there are two FDA approved atypical antipsychotic medications that treat irritability in children with autism. These are aripiprazole and risperidone. While it is thought that aripiprazole may cause less weight gain than risperidone, clinically this has not been proven.

Understanding the relative risk of ATAP-induced weight gain that results from risperidone versus aripiprazole in a real-world setting could help guide the choice of medical intervention and reduce the cardiometabolic risks, and, most critically, address the limitations of current studies, which have not been able to provide clear clinical insights given the difficulty with having a representative and robust number of patients enrolled.

To be enrolled in this study, participants must be younger than 18 years of age, on the autism spectrum, have behavioral dysregulation, be naive to treatment with atypical antipsychotics and be seen either in the Division of Developmental Medicine or Child and Adolescent Psychiatry at Vanderbilt University Medical Center.

For enrolled patients, the ordering provider will see an order set, randomized to either aripiprazole or risperidone. They will then choose the recommended antipsychotic that the patient has been randomized to, or override the prompt. If the provider overrides the prompt, they will be asked to provide a reason for not choosing the recommended option.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Other
Masking
None

Eligibility Criteria

Ages
— to 17 Years (Child)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • age 17 years and younger
  • diagnosed with autism
  • have behavior problems
  • seen in Vanderbilt clinic
  • naïve to atypical antipsychotics

Exclusion Criteria

  • 18 years or older
  • history of atypical antipsychotic use
  • not diagnosed with autism

Arms & Interventions

Treatment with Risperidone

Active Comparator

Patients prescribed Risperidone

Intervention: Comparison of Risperidone and Aripiprazole (Drug)

Treatment with Aripiprazole

Active Comparator

Patients prescribed Aripiprazole

Intervention: Comparison of Risperidone and Aripiprazole (Drug)

Outcomes

Primary Outcomes

weight gain

Time Frame: 3 months

change in weight

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Angela Maxwell-Horn

Assistant Professor of Pediatrics

Vanderbilt University Medical Center

Study Sites (1)

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