Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT00585169 · ClinicalTrials.gov registry record · Phase 2

Memantine Treatment Study of Pathological Gambling

A Phase 2 study of Pathological Gambling, sponsored by Yale University.

Completed
Registry status
Phase 2
Development phase
29
Enrollment target
2
Study locations

NCT00585169: Completed Phase 2 study of Pathological Gambling, sponsored by Yale University.

NCT00585169 is a Phase 2 study of Pathological Gambling that has completed, run by Yale University. The registered enrollment target is 29 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (78% lower). The trial reports 2 study locations across 2 states. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00585169, a Phase 2 study of Pathological Gambling, has completed, sponsored by Yale University.

COMPLETED
Registry status
Phase 2
Development phase
29 participants
Enrollment target
2
Study locations

Study Summary

The goal of the proposed study is to evaluate the efficacy and safety of the drug memantine in individuals with pathological gambling (PG). Thirty subjects with DSM-IV PG will receive 10 weeks of open-label treatment with memantine. The hypothesis to be tested is that memantine will be effective and well tolerated in patients with PG. We hypothesize that memantine will reduce the severity of gambling symptoms and improve patients' overall functioning. This study will provide needed data on the treatment of a disabling disorder that currently lacks a clearly effective treatment.

Primary Outcome

The PGYBOCS is a reliable \& valid, 10-item, clinician administered scale that rates gambling symptoms within the last 7 days. The first 5 questions assess urges and thoughts associated with pathological gambling, and the last 5 questions assess the behavioral component of the disorder. Scores of 0 through 4 are assigned each item according to the severity of the response (0 = least severe response or none, 4 = most severe response or extreme)with a score ranging from 0-40. Each set of questions

Conditions Studied

Interventions

  • DRUG Memantine Hydrochloride

Study Locations (2)

Connecticut

  • Yale University School of Medicine - New Haven

Minnesota

  • University of Minnesota Medical Center, Fairview - Minneapolis

Trial Details

FieldValue
Enrollment Target 29 participants
Start Date 2007-12
Est. Completion 2011-12
Phase Phase 2
Yale University

1,492 total trials

What the finished NCT00585169 record still lists

NCT00585169 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 29 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (78% lower).

The record links to 1 condition, with Pathological Gambling appearing as the primary indexed condition, and to 1 intervention - of which Memantine Hydrochloride is the first listed.

NCT00585169 reports a single indexed study location in Connecticut, Minnesota.

Frequently Asked Questions

What is clinical trial NCT00585169 about?

NCT00585169 is a clinical study titled "Memantine Treatment Study of Pathological Gambling". The goal of the proposed study is to evaluate the efficacy and safety of the drug memantine in individuals with pathological gambling (PG). Thirty subjects with DSM-IV PG will receive 10 weeks of open-label treatment with memantine. The hypothesis to be tested is that memantine will be effective and...

What is the current status of trial NCT00585169?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 29 participants. The study started on 2007-12. Estimated completion is 2011-12.

What conditions does trial NCT00585169 study?

This clinical trial studies the following conditions: Pathological Gambling.

What interventions are being tested in trial NCT00585169?

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

Who is sponsoring clinical trial NCT00585169?

This trial is sponsored by Yale University, which has 1,492 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00585169 being conducted?

This trial has 2 study locations across Connecticut, Minnesota. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Pathological Gambling

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT00585169's enrollment target sits among peer trials

29 1669th of 2000 higher than 324 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 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

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT02429557 · 29 participants · Phase 1

    Hemodynamic Mechanisms of Abdominal Compression in the Treatment of Orthostatic Hypotension in Autonomic Failure

  • NCT02568878 · 29 participants · Phase 3

    Creatine for Depressed Male and Female Methamphetamine Users

  • NCT03014401 · 29 participants · NA

    The Effect of Adipose-Derived Stem Cells for Knee Osteoarthritis

  • NCT03128996 · 29 participants · Phase 1

    Reduced Intensity Conditioning and Familial HLA-Mismatched BMT for Non-Malignant Disorders

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT00585169, the US trial registry maintained by the National Library of Medicine. NCT00585169 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.