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Completed Phase 3 Interventional

Subject Information and Consent Form F1J-US-HMCB Duloxetine Once-Daily Dosing Versus Placebo in Patients With Major Depression and Pain

ClinicalTrials.gov ID: NCT00036335

Public ClinicalTrials.gov record NCT00036335. 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 15, 2026, 6:32 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

Duloxetine Hydrochloride (LY248686) Protocol F1J-US-HMCB Duloxetine Once-Daily Dosing Versus Placebo in Patients With Major Depression and Pain

Study identification

NCT ID
NCT00036335
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Eli Lilly and Company
Industry
Enrollment
286 participants

Conditions and interventions

Interventions

  • Duloxetine Hydrochloride Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
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
Feb 28, 2002
Primary completion
Not listed
Completion
Dec 31, 2002
Last update posted
Jul 18, 2006

2002 – 2003

United States locations

U.S. sites
25
U.S. states
17
U.S. cities
25
Facility City State ZIP Site status
Not listed Peoria Arizona
Not listed Burbank California
Not listed Fresno California
Not listed St. Petersburg Florida
Not listed West Palm Beach Florida
Not listed Atlanta Georgia
Not listed Oakbrook Terrace Illinois
Not listed Springfield Illinois
Not listed Glen Burnie Maryland
Not listed Farmington Hills Michigan
Not listed Nashua New Hampshire
Not listed Clementon New Jersey
Not listed Moorestown New Jersey
Not listed Albany New York
Not listed Olean New York
Not listed Cincinnati Ohio
Not listed Toledo Ohio
Not listed Philadelphia Pennsylvania
Not listed Austin Texas
Not listed Lake Jackson Texas
Not listed San Antonio Texas
Not listed Woodstock Vermont
Not listed Richmond Virginia
Not listed Seattle Washington
Not listed Brown Deer Wisconsin

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 NCT00036335, 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 Jul 18, 2006 · Synced May 15, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00036335 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →