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Trial · NCT01411085

Risperidone and Desipramine in Alcohol Use and Schizophrenia

NCT01411085, Phase 2, Completed, Dartmouth-Hitchcock Medical Center; results first posted 2018-03-23

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Risperidone and Desipramine in Alcohol Use and Schizophrenia. Trials, record NCT01411085. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT01411085

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Trial

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

Title
Risperidone and Desipramine in Alcohol Use and Schizophrenia
NCT number
NCT01411085
Status
Completed
Phases
Phase 2
Enrollment
12 participants, actual
Lead sponsor
Dartmouth-Hitchcock Medical Center
Conditions
Schizophrenia, Alcoholism, Dual Diagnosis
Interventions
Risperidone + Desipramine
First posted
2011-08-08
Last updated
2018-03-23
Results first posted
2018-03-23

Source ClinicalTrials.gov

Registered outcomes1

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

ListOutcomeTime frameDescription
PrimaryTimeline Followback Assessing Number of Drinks Per WeekWeekly for 14 weeks, using data from last 8 weeks
Alcohol/other substance use (including tobacco) will be assessed primarily by weekly self-report using the Timeline Followback (TLFB) method enhanced by procedures to strengthen the reliability and validity of this measure. It involves asking participants to retrospectively estimate their alcohol and other substance use.

Outcomes1

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

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYTimeline Followback Assessing Number of Drinks Per WeekWeekly for 14 weeks, using data from last 8 weeksThe analysis was performed on all completers (N=7).Drinks per weekMEAN

Results by group1

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

OutcomeGroupCategoryValueSpreadUnits
Timeline Followback Assessing Number of Drinks Per WeekRisperidone + Desipramine35.9Standard Deviation 20.4Drinks per week

Participant flow3

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

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDRisperidone + Desipramine10
Overall StudyCOMPLETEDRisperidone + Desipramine7
Overall StudyNOT COMPLETEDRisperidone + Desipramine3

Adverse events29

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

TypeEventOrgan systemGroupAffectedAt riskEvents
otherAnxietyPsychiatric disordersRisperidone + Desipramine1102
otherDepressionPsychiatric disordersRisperidone + Desipramine1101
otherDiarreheaGastrointestinal disordersRisperidone + Desipramine1101
otherDizzinessGeneral disordersRisperidone + Desipramine1101
otherDry MouthGastrointestinal disordersRisperidone + Desipramine2102
otherFallInjury, poisoning and procedural complicationsRisperidone + Desipramine2102
otherGum InfectionInfections and infestationsRisperidone + Desipramine1101
otherHypertensionCardiac disordersRisperidone + Desipramine1101
otherIncreased appetiteGastrointestinal disordersRisperidone + Desipramine1101
otherInsomniaPsychiatric disordersRisperidone + Desipramine1101

Adverse event totals3

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityRisperidone + Desipramine
Total, other adverse eventsRisperidone + Desipramine1010
Total, serious adverse eventsRisperidone + Desipramine310

Papers0

The papers the trial lists on ClinicalTrials.gov.

None in this release.

Grants1

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.

ProjectTitlePrincipal investigatorsOrganizationFunderFiscal years
R21AA019534Alcoholism and Schizophrenia: A Translational Approach to TreatmentGREEN, ALAN IDARTMOUTH COLLEGENATIONAL INSTITUTE ON ALCOHOL ABUSE AND ALCOHOLISM2011 to 2012

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/NCT01411085

GET https://conductscience.org/api/trials/v1/NCT01411085/events?page=2