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Terminated Phase 3 Interventional

A Ten-Week Study Evaluating The Effectiveness And Safety Of Zoloft In Children And Adolescents With A Diagnosis Of PTSD

ClinicalTrials.gov ID: NCT00150306

Public ClinicalTrials.gov record NCT00150306. 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 Sep 30, 2026, 4:06 PM 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 Multicenter, 10-Week, Randomized, Double-Blind Study Of Sertraline And Placebo In Children And Adolescents With Posttraumatic Stress Disorder (PTSD)

Brief summary

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

To evaluate the safety and efficacy of sertraline compared to placebo in children and adolescents (6 to 17 years of age) who are outpatients with Posttraumatic Stress Disorder.

Study identification

NCT ID
NCT00150306
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Enrollment
160 participants

Conditions and interventions

Eligibility (public fields only)

Age range
6 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
Nov 2002 (Type not available)
Primary completion
Not listed
Completion
Jul 2007 (Actual)
Last update posted
Jan 29, 2021

2002 – 2007

United States locations

U.S. sites
23
U.S. states
14
U.S. cities
23
Facility City State ZIP Site status
Pfizer Investigational Site Scottsdale Arizona 85281 —
Pfizer Investigational Site Sacramento California 95817 —
Pfizer Investigational Site San Diego California 92111 —
Pfizer Investigational Site San Marcos California 92078 —
Pfizer Investigational Site Washington D.C. District of Columbia 20010 —
Pfizer Investigational Site Gainesville Florida 32611 —
Pfizer Investigational Site Indianapolis Indiana 46202-5200 —
Pfizer Investigational Site Terre Haute Indiana 47802 —
Pfizer Investigational Site Overland Park Kansas 66214 —
Pfizer Investigational Site Baton Rouge Louisiana 70816 —
Pfizer Investigational Site New Orleans Louisiana 70112 —
Pfizer Investigational Site Bethesda Maryland 20814 —
Pfizer Investigational Site Las Vegas Nevada 89128 —
Pfizer Investigational Site Lebanon New Hampshire 03756-0002 —
Pfizer Investigational Site Manhasset New York 11030 —
Pfizer Investigational Site New York New York 10016 —
Pfizer Investigational Site Stony Brook New York 11794 —
Pfizer Investigational Site Cleveland Ohio 44106 —
Pfizer Investigational Site Lyndhurst Ohio 44124 —
Pfizer Investigational Site Charleston South Carolina 29425 —
Pfizer Investigational Site Galveston Texas 77555-0188 —
Pfizer Investigational Site Houston Texas 77058 —
Pfizer Investigational Site Plano Texas 75024 —

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 NCT00150306, 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 Jan 29, 2021 · Synced Sep 30, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00150306 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →