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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT03735888
Other study ID # IRB-44589
Secondary ID
Status Not yet recruiting
Phase Phase 2
First received
Last updated
Start date November 2018
Est. completion date December 2020

Study information

Verified date November 2018
Source Stanford University
Contact Robin Libove
Phone (650)736-1235
Email rlibove@stanford.edu
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Autism is a pervasive developmental disorder characterized by core deficits in social behavior and communication and the presence of repetitive/stereotyped behaviors. The objective of the study is to evaluate the efficacy of Esomeprazole as a treatment for social communication deficits in children with Autism Spectrum Disorder (ASD). This prospective 12 week open-label study will invite 25 children with ASD between the ages of 2 and 6 years of age to participate.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 25
Est. completion date December 2020
Est. primary completion date December 2020
Accepts healthy volunteers No
Gender All
Age group 2 Years to 6 Years
Eligibility Inclusion Criteria:

- outpatients 2 to 6 years of age;

- males and females who are physically healthy;

- diagnosis of autism spectrum disorder based on clinical evaluation and DSM-5 criteria, and confirmed using the Autism Diagnostic Interview-Revised, and the Autism Diagnostic Observation Schedule;

- care provider who could reliably bring subject to clinic visits, could provide trustworthy ratings, and interacted with subject on a regular basis;

- ability of subject to swallow the compound;

- stable concomitant medications for at least 2 weeks (4 weeks if patient took fluoxetine);

- no planned changes in psychosocial interventions during the open-label trial.

Exclusion Criteria:

- DSM-5 diagnosis of schizophrenia, schizoaffective disorder, or psychotic disorder not otherwise specified;

- prior adequate trial of Esomeprazole;

- active medical problems such as unstable seizures, or significant physical illness (e.g., serious liver or renal pathology).

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Esomeprazole
Esomeprazole (oral)

Locations

Country Name City State
n/a

Sponsors (2)

Lead Sponsor Collaborator
Stanford University SPARK (Stanford University)

Outcome

Type Measure Description Time frame Safety issue
Primary Change on Social Responsiveness Scale, 2nd Edition (SRS-2) Baseline, 4 Weeks, 8 Weeks
Secondary Change on Aberrant Behavior Checklist, 2nd Edition (ABC-2) Baseline, 4 Weeks, 8 Weeks
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