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Trial · NCT01215357

Clinical Study to Determine if Ecopipam Can Reduce Urges to Gamble

NCT01215357, Phase 2, Completed, Emalex Biosciences Inc.; results first posted 2013-02-12

3 sourcestrials-2026-11-12-0.4.0

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ConductScience Library. Clinical Study to Determine if Ecopipam Can Reduce Urges to Gamble. Trials, record NCT01215357. Release trials-2026-11-12-0.4.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT01215357

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Clinical Study to Determine if Ecopipam Can Reduce Urges to Gamble
NCT number
NCT01215357
Status
Completed
Phases
Phase 2
Enrollment
34 participants, actual
Lead sponsor
Emalex Biosciences Inc.
Conditions
Pathological Gambling
Interventions
Ecopipam
First posted
2010-10-06
Last updated
2024-05-14
Results first posted
2013-02-12
Limitations and caveats
This was an open label trial of ecopipam for the treatment of pathological gambling. A significant effect of drug treatment was demonstrated. These data need to be verified with a double-blind, placebo controlled trial.

Source ClinicalTrials.gov

Registered outcomes4

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryStatistically Significant (p<0.05) Decrease From Baseline in Yale Brown Obsessive Compulsive Scale Modified for Pathological GamblingBaseline and 6 weeks
This scale assesses the severity of gambling urges and gambling behaviors. The study anticipates that there will be a reduction in either or both of these assessments. The range is from a minimum of 0 to a maximum of 40, where zero means no gambling urges occurred.
SecondaryType, Frequency and Severity of Side Effects6 weeksAll side effects of the drug will be monitored and recorded
SecondaryStatistically Significant Changes in the Gambling Symptom Assessment Scale6 weeksIt is expected that there will be decreases in this scale
SecondaryEffects on the Clinical Global Impression6 weeksClinician's Global Impression is used assess severity and changes in clinical symptoms during and at the end of the study

Outcomes4

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYStatistically Significant (p<0.05) Decrease From Baseline in Yale Brown Obsessive Compulsive Scale Modified for Pathological GamblingBaseline and 6 weeksPatients completing all visitsYBOCS scoreMEAN
SECONDARYType, Frequency and Severity of Side Effects6 weeks
SECONDARYStatistically Significant Changes in the Gambling Symptom Assessment Scale6 weeks
SECONDARYEffects on the Clinical Global Impression6 weeks

Results by group1

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnits
Statistically Significant (p<0.05) Decrease From Baseline in Yale Brown Obsessive Compulsive Scale Modified for Pathological GamblingEcopipam 50 mg or 100 mg as Needed13.9Standard Deviation 8.79YBOCS score

Participant flow3

How many started, completed or left each group, period by period.

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDEcopipam (50 or 100 mg, as Needed)34
Overall StudyCOMPLETEDEcopipam (50 or 100 mg, as Needed)22
Overall StudyNOT COMPLETEDEcopipam (50 or 100 mg, as Needed)12

Adverse events5

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

TypeEventOrgan systemGroupAffectedAt riskEvents
otherSedationNervous system disordersEcopipam 50 or 100 mg, as Needed4344
otherAnxietyNervous system disordersEcopipam 50 or 100 mg, as Needed3343
otherConstipationGastrointestinal disordersEcopipam 50 or 100 mg, as Needed2342
otherRhinorrheaEye disordersEcopipam 50 or 100 mg, as Needed2342
otherVomitingGastrointestinal disordersEcopipam 50 or 100 mg, as Needed2342

Adverse event totals3

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityEcopipam 50 or 100 mg, as Needed
Total, other adverse eventsEcopipam 50 or 100 mg, as Needed1334
Total, serious adverse eventsEcopipam 50 or 100 mg, as Needed034

Papers1

The papers the trial lists on ClinicalTrials.gov.

PMIDListed as
25166480DERIVED

Source PubMed

Grants0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

None in this release.

Trial comparisons0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

None in this release.

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT01215357

GET https://conductscience.org/api/trials/v1/NCT01215357/registered