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Completed Phase 4 Interventional Results available

A Study of Escitalopram in the Treatment of Children and Adolescents With Generalized Anxiety Disorder

ClinicalTrials.gov ID: NCT03924323

Public ClinicalTrials.gov record NCT03924323. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 22, 2026, 6:58 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomized, Multicenter, Double-Blind, Flexibly-dosed, Efficacy and Safety Study of Escitalopram in the Treatment of Children and Adolescents With Generalized Anxiety Disorder

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This is a study in minors (7 to 17 years old) diagnosed with generalized anxiety disorder (GAD) and evaluated using standard questionnaires as having at least moderate severity of GAD. Participating minors will be assigned to receive either the study drug escitalopram or a pill without any drug in it called a placebo. The purpose of this research is to study the safety and effectiveness of escitalopram in minors with GAD.

Study identification

NCT ID
NCT03924323
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
AbbVie
Industry
Enrollment
273 participants

Conditions and interventions

Interventions

Drug · Other

Eligibility (public fields only)

Age range
7 Years to 17 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
May 30, 2019 (Actual)
Primary completion
Sep 20, 2021 (Actual)
Completion
Sep 20, 2021 (Actual)
Last update posted
Nov 14, 2022

2019 – 2021

United States locations

U.S. sites
39
U.S. states
18
U.S. cities
38
Facility City State ZIP Site status
Harmonex /ID# 233342 Dothan Alabama 36303 —
Woodland International Research Group /ID# 233348 Little Rock Arkansas 72211 —
Woodland Research Northwest, LLC /ID# 233366 Rogers Arkansas 72758-6442 —
ATP Clinical Research, Inc /ID# 233362 Costa Mesa California 92626-4607 —
ProScience Research Group /ID# 233374 Culver City California 90230-6632 —
Sun Valley Research Center /ID# 233343 Imperial California 92251-9401 —
MCB Clinical Research Centers /ID# 233372 Colorado Springs Colorado 80910 —
Emerson Clinical Research Inst /ID# 233371 Washington D.C. District of Columbia 20011 —
Innovative Clinical Research /ID# 233365 Fort Lauderdale Florida 33319 —
Indago Research and Health Cen /ID# 233364 Hialeah Florida 33012-4170 —
CNS Healthcare - Jacksonville /ID# 233352 Jacksonville Florida 32256-6039 —
Accel Research Sites-Maitland Clinical Research Unit /ID# 233368 Maitland Florida 32751 —
Medical Research Group of Central Florida /ID# 233357 Orange City Florida 32763 —
Clinical Neuroscience Solutions, Inc /ID# 233350 Orlando Florida 32801-2986 —
APG Research, LLC /ID# 233337 Orlando Florida 32803 —
University of South Florida Rothman Center of Neuropsychiatry /ID# 233356 St. Petersburg Florida 33701-4708 —
Capstone Clinical Research /ID# 233354 Libertyville Illinois 60048-5341 —
Baber Research Group /ID# 233363 Naperville Illinois 60563-6502 —
Psychiatric Associates /ID# 233360 Overland Park Kansas 66221 —
Alivation Research /ID# 233338 Lincoln Nebraska 68526-9474 —
Center for Psychiatry and Behavioral Medicine Inc /ID# 233355 Las Vegas Nevada 89128-0819 —
Manhattan Behavioral Medicine PLLC /ID# 233351 New York New York 10036 —
Finger Lakes Clinical Research /ID# 233347 Rochester New York 14618-1609 —
Quest Therapeutics of Avon Lake /ID# 233367 Avon Lake Ohio 44012 —
Neuro-Behavioral Clinical Research, Inc. /ID# 233375 Canton Ohio 44720 —
University of Cincinnati /ID# 233341 Cincinnati Ohio 45219 —
UH Cleveland Medical Center /ID# 233373 Cleveland Ohio 44106 —
Midwest Clinical Research Center /ID# 233346 Dayton Ohio 45417 —
CincyScience /ID# 233359 West Chester Ohio 45069 —
SP Research, PLLC /ID# 233340 Oklahoma City Oklahoma 73112-8729 —
Central States Research /ID# 233339 Tulsa Oklahoma 74136 —
Coastal Carolina Research Center /ID# 233344 North Charleston South Carolina 29405 —
Houston Clinical Trials /ID# 233345 Bellaire Texas 77401-2928 —
Relaro Medical Trials /ID# 233369 Dallas Texas 75243 —
AIM Trials /ID# 233361 Plano Texas 75093 —
Focus Center, PC /ID# 233349 Ogden Utah 84405-4946 —
University of Virginia /ID# 233370 Charlottesville Virginia 22903 —
Northwest Clinical Research Center /ID# 233358 Bellevue Washington 98007 —
Core Clinical Research /ID# 233353 Everett Washington 98201 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03924323, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Nov 14, 2022 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03924323 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →