ClinicalTrials.gov record
Completed Phase 4 Interventional Results available

Escitalopram in the Treatment of Dysthymic Disorder, Double Blind

ClinicalTrials.gov ID: NCT00220701

Public ClinicalTrials.gov record NCT00220701. 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 May 7, 2026, 9:04 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

Double-Blind Placebo-Controlled Study of Escitalopram in the Treatment of Dysthymic Disorder

Study identification

NCT ID
NCT00220701
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
St. Luke's-Roosevelt Hospital Center
Other
Enrollment
36 participants

Conditions and interventions

Interventions

  • Lexapro (escitalopram) Drug

Drug

Eligibility (public fields only)

Age range
18 Years to 65 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 31, 2002
Primary completion
Oct 31, 2008
Completion
Dec 31, 2008
Last update posted
Nov 10, 2015

2002 – 2009

United States locations

U.S. sites
1
U.S. states
1
U.S. cities
1
Facility City State ZIP Site status
Mood Disorders Research Program, St. Luke's-Roosevelt Hospital Center New York New York 10019

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 NCT00220701, 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 10, 2015 · Synced May 7, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00220701 live on ClinicalTrials.gov.

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