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Trial · NCT00062738

Treatment of Depression in Parkinson's Disease Trial

NCT00062738, Phase 2, Completed, Rutgers, The State University of New Jersey; results first posted 2013-03-05

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Treatment of Depression in Parkinson's Disease Trial. Trials, record NCT00062738. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT00062738

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Trial

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

Title
Treatment of Depression in Parkinson's Disease Trial
NCT number
NCT00062738
Status
Completed
Phases
Phase 2
Enrollment
52 participants, actual
Lead sponsor
Rutgers, The State University of New Jersey
Conditions
Parkinson Disease, Depression
Interventions
paroxetine, Nortriptyline, placebo
First posted
2003-06-13
Last updated
2015-11-24
Results first posted
2013-03-05
Limitations and caveats
This was only an eight week trial with relatively few participants.

Source ClinicalTrials.gov

Registered outcomes2

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

ListOutcomeTime frameDescription
PrimaryHamilton Depression Scale8 weekstotal score on HDRS (0-54 higher score is worse)
SecondaryPercent Responders8 weeksPercent of patients who had a 50% decrease in total HDRS at 8 weeks

Outcomes2

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

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYHamilton Depression Scale8 weeksintent to treat - total patients in the armunits on a scaleLEAST_SQUARES_MEAN
SECONDARYPercent Responders8 weeksintent to treatpercent of patients who were respondersNUMBER

Results by group6

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

OutcomeGroupCategoryValueSpreadUnits
Hamilton Depression ScaleNortriptyline10.84Standard Deviation 6.2units on a scale
Hamilton Depression ScaleParoxetine12.45Standard Deviation 6.36units on a scale
Hamilton Depression ScalePlacebo15.81Standard Deviation 5.78units on a scale
Percent RespondersNortriptyline53percent of patients who were responders
Percent RespondersParoxetine11percent of patients who were responders
Percent RespondersPlacebo24percent of patients who were responders

Participant flow9

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

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDNortriptyline17
Overall StudySTARTEDParoxetine18
Overall StudySTARTEDPlacebo17
Overall StudyCOMPLETEDNortriptyline17
Overall StudyCOMPLETEDParoxetine18
Overall StudyCOMPLETEDPlacebo17
Overall StudyNOT COMPLETEDNortriptyline0
Overall StudyNOT COMPLETEDParoxetine0
Overall StudyNOT COMPLETEDPlacebo0

Adverse events27

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

TypeEventOrgan systemGroupAffectedAt riskEvents
otherconstipationGastrointestinal disordersNortriptyline6176
otherconstipationGastrointestinal disordersParoxetine1181
otherconstipationGastrointestinal disordersPlacebo1171
otherdry mouthGastrointestinal disordersNortriptyline7177
otherdry mouthGastrointestinal disordersParoxetine1181
otherdry mouthGastrointestinal disordersPlacebo0170
otherinsomniaNervous system disordersNortriptyline2172
otherinsomniaNervous system disordersParoxetine0180
otherinsomniaNervous system disordersPlacebo4174
otherfatigueGeneral disordersNortriptyline0170

Adverse event totals9

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityNortriptyline
Total, all-cause mortalityParoxetine
Total, all-cause mortalityPlacebo
Total, other adverse eventsNortriptyline1717
Total, other adverse eventsParoxetine718
Total, other adverse eventsPlacebo1117
Total, serious adverse eventsNortriptyline017
Total, serious adverse eventsParoxetine118
Total, serious adverse eventsPlacebo217

Papers3

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource
19092112RESULTPubMed
20463113DERIVEDPubMed
20808132DERIVEDPubMed

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/NCT00062738

GET https://conductscience.org/api/trials/v1/NCT00062738/events?page=2