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NCT00036335 · ClinicalTrials.gov registry record · Phase 3

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

A Phase 3 study, sponsored by Eli Lilly and Company.

Completed
Registry status
Phase 3
Development phase
286
Enrollment target

NCT00036335: Completed Phase 3 study, sponsored by Eli Lilly and Company.

NCT00036335 is a Phase 3 study that has completed, run by Eli Lilly and Company. The registered enrollment target is 286 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (63% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00036335, a Phase 3 study, has completed, sponsored by Eli Lilly and Company.

COMPLETED
Registry status
Phase 3
Development phase
286 participants
Enrollment target

Study Summary

The purposes of this study are to determine whether an investigational drug can help patients suffering from major depression with pain symptoms, and gather data on the safety of the investigational drug including any side effects that might be associated with it.

Interventions

  • DRUG Duloxetine Hydrochloride

Trial Details

FieldValue
Enrollment Target 286 participants
Start Date 2002-03
Est. Completion 2003-01
Phase Phase 3
Eli Lilly and Company

1,341 total trials

What the finished NCT00036335 record still lists

NCT00036335 is an interventional study that assigns participants to a tested intervention. The registered 286 participants enrollment target is mid-sized for trials with a published cap, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (63% lower).

The record links to 0 conditions, and to 1 intervention - of which Duloxetine Hydrochloride is the first listed.

NCT00036335 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00036335 about?

NCT00036335 is a clinical study titled "Subject Information and Consent Form F1J-US-HMCB Duloxetine Once-Daily Dosing Versus Placebo in Patients With Major Depression and Pain". The purposes of this study are to determine whether an investigational drug can help patients suffering from major depression with pain symptoms, and gather data on the safety of the investigational drug including any side effects that might be associated with it.

What is the current status of trial NCT00036335?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 286 participants. The study started on 2002-03. Estimated completion is 2003-01.

What interventions are being tested in trial NCT00036335?

The interventions under investigation include: Duloxetine Hydrochloride (DRUG).

Who is sponsoring clinical trial NCT00036335?

This trial is sponsored by Eli Lilly and Company, which has 1,341 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00036335's enrollment target sits among peer trials

286 1182nd of 2000 higher than 816 of 2,000 other Phase 3 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 3 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT00036335, the US trial registry maintained by the National Library of Medicine. NCT00036335 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.