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NCT00190736 · ClinicalTrials.gov registry record · Phase 4

Efficacy and Safety of Once-Daily Atomoxetine Hydrochloride in Adults With ADHD Over an Extended Period of Time (6 Months)

A Phase 4 study, sponsored by Eli Lilly and Company.

Completed
Registry status
Phase 4
Development phase
440
Enrollment target

NCT00190736 is a Phase 4 study that has completed, run by Eli Lilly and Company. The registered enrollment target is 440 participants.

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The verdict

NCT00190736, a Phase 4 study, has completed, sponsored by Eli Lilly and Company.

COMPLETED
Registry status
Phase 4
Development phase
440 participants
Enrollment target

Study Summary

A study to compare the effect of once-daily atomoxetine versus placebo in treating symptoms of ADHD in adults for up to 6 months.

Interventions

  • DRUG placebo
  • DRUG Atomoxetine Hydrochloride

Trial Details

FieldValue
Enrollment Target 440 participants
Start Date 2004-09
Est. Completion 2006-09
Phase Phase 4

Sponsor

Eli Lilly and Company

1,341 total trials

What the Registry Record Tells You About NCT00190736

The ClinicalTrials.gov registry entry for NCT00190736 describes a study currently listed as completed, categorized as Phase 4. The registered enrollment target is 440 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Eli Lilly and Company, which has 1,341 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which placebo is the first listed.

NCT00190736 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00190736 about?

NCT00190736 is a clinical study titled "Efficacy and Safety of Once-Daily Atomoxetine Hydrochloride in Adults With ADHD Over an Extended Period of Time (6 Months)". A study to compare the effect of once-daily atomoxetine versus placebo in treating symptoms of ADHD in adults for up to 6 months.

What is the current status of trial NCT00190736?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 440 participants. The study started on 2004-09. Estimated completion is 2006-09.

What interventions are being tested in trial NCT00190736?

The interventions under investigation include: placebo (DRUG), Atomoxetine Hydrochloride (DRUG).

Who is sponsoring clinical trial NCT00190736?

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

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.