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NCT02141113 · ClinicalTrials.gov registry record · Phase 4

Efficacy and Safety Eval of Guanfacine Hydrochloride in Combination With Psychostimulants in Adults (18-65).

A Phase 4 study of Adult Attention Deficit Hyperactivity Disorder, sponsored by Rochester Center for Behavioral Medicine.

Completed
Registry status
Phase 4
Development phase
26
Enrollment target
1
Study location

NCT02141113 is a Phase 4 study of Adult Attention Deficit Hyperactivity Disorder that has completed, run by Rochester Center for Behavioral Medicine. The registered enrollment target is 26 participants. The trial reports 1 study location across 1 state.

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The verdict

NCT02141113, a Phase 4 study of Adult Attention Deficit Hyperactivity Disorder, has completed, sponsored by Rochester Center for Behavioral Medicine.

COMPLETED
Registry status
Phase 4
Development phase
26 participants
Enrollment target
1
Study location

Study Summary

This is considered an investigator-initiated clinical research trial, which means that your study doctor is researching a particular medication (in this case a medication that is currently FDA- approved) for the treatment of AD/HD in individuals ages 6-17. The medication is guanfacine hydrochloride. The hypothesis is that this medication could be used in adults with Attention Deficit/Hyperactivity Disorder who have not received satisfactory results with their current stimulant ADHD medication. The study drug is investigational for use in adults. Investigational means it has not been approved by the U.S. Food and Drug Administration (FDA) for use in adults.

Interventions

  • OTHER Placebo
  • DRUG Guanfacine Hydrochloride

Study Locations (1)

Michigan

  • Rochester Center for Behavioral Medicine - Rochester Hills

Trial Details

FieldValue
Enrollment Target 26 participants
Start Date 2012-11
Est. Completion 2014-11
Phase Phase 4

What the Registry Record Tells You About NCT02141113

The ClinicalTrials.gov registry entry for NCT02141113 describes a study currently listed as completed, categorized as Phase 4. The registered enrollment target is 26 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Rochester Center for Behavioral Medicine, which has 4 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Adult Attention Deficit Hyperactivity Disorder appearing as the primary indexed condition, and to 2 interventions - of which Placebo is the first listed.

NCT02141113 reports 1 study location spanning 1 distinct geographic area - top geographies include Michigan.

Frequently Asked Questions

What is clinical trial NCT02141113 about?

NCT02141113 is a clinical study titled "Efficacy and Safety Eval of Guanfacine Hydrochloride in Combination With Psychostimulants in Adults (18-65).". This is considered an investigator-initiated clinical research trial, which means that your study doctor is researching a particular medication (in this case a medication that is currently FDA- approved) for the treatment of AD/HD in individuals ages 6-17. The medication is guanfacine hydrochloride....

What is the current status of trial NCT02141113?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 26 participants. The study started on 2012-11. Estimated completion is 2014-11.

What conditions does trial NCT02141113 study?

This clinical trial studies the following conditions: Adult Attention Deficit Hyperactivity Disorder.

What interventions are being tested in trial NCT02141113?

The interventions under investigation include: Placebo (OTHER), Guanfacine Hydrochloride (DRUG).

Who is sponsoring clinical trial NCT02141113?

This trial is sponsored by Rochester Center for Behavioral Medicine, which has 4 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT02141113 being conducted?

This trial has 1 study location across Michigan. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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