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Trial · NCT01472874

Single Daily Dosage of Trientine for Maintenance Treatment for Wilson Disease

NCT01472874, Not applicable, Completed, Yale University; results first posted 2014-05-19

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Single Daily Dosage of Trientine for Maintenance Treatment for Wilson Disease. Trials, record NCT01472874. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT01472874

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Trial

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

Title
Single Daily Dosage of Trientine for Maintenance Treatment for Wilson Disease
NCT number
NCT01472874
Status
Completed
Phases
Not applicable
Enrollment
8 participants, actual
Lead sponsor
Yale University
Conditions
Wilson Disease
Interventions
Once a day Trientine
First posted
2011-11-17
Last updated
2020-04-15
Results first posted
2014-05-19

Source ClinicalTrials.gov

Registered outcomes12

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

ListOutcomeTime frameDescription
PrimaryALTPre Treatment (mean)Alanine transaminase
PrimaryALTMonths 1,2,3,6,9,12 (mean)Alanine transaminase
PrimaryCu SerumPre Treatment (mean)
PrimaryCu SerumMonths 1,2,3,6,9,12 (mean)
SecondaryINRPre Treatment (mean)
The International Normalized Ratio (INR) is a standard way to describe the time it takes for blood to clot; an INR range of 0.8 to 1.2 is considered normal for a healthy person who is not using oral anticoagulant therapy
SecondaryINRMonths 1,2,3,6,9,12 (mean)
The International Normalized Ratio (INR) is a standard way to describe the time it takes for blood to clot; an INR range of 0.8 to 1.2 is considered normal for a healthy person who is not using oral anticoagulant therapy
SecondaryAlbuminPre Treatment (mean)
SecondaryAlbuminMonths 1,2,3,6,9,12 (mean)
SecondaryCu UrinePre Treatment (mean)
SecondaryCu UrineMonths 1,2,3,6,9,12 (mean)

Outcomes12

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

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYALTPre Treatment (mean)U/LMEAN
PRIMARYALTMonths 1,2,3,6,9,12 (mean)U/LMEAN
SECONDARYINRPre Treatment (mean)international normalized ratioMEAN
SECONDARYINRMonths 1,2,3,6,9,12 (mean)international normalized ratioMEAN
SECONDARYAlbuminPre Treatment (mean)g/dLMEAN
SECONDARYAlbuminMonths 1,2,3,6,9,12 (mean)g/dLMEAN
PRIMARYCu SerumPre Treatment (mean)mcg/24hMEAN
PRIMARYCu SerumMonths 1,2,3,6,9,12 (mean)mcg/24hMEAN
SECONDARYCu UrinePre Treatment (mean)mcg/24hrMEAN
SECONDARYCu UrineMonths 1,2,3,6,9,12 (mean)mcg/24hrMEAN

Results by group12

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

OutcomeGroupCategoryValueSpreadUnits
ALTOnce a Day Trientine41.38Standard Deviation 31.81U/L
ALTOnce a Day Trientine50.89Standard Deviation 32.29U/L
INROnce a Day Trientine0.99Standard Deviation 0.07international normalized ratio
INROnce a Day Trientine1.05Standard Deviation 0.08international normalized ratio
AlbuminOnce a Day Trientine0.54Standard Deviation 0.30g/dL
AlbuminOnce a Day Trientine0.52Standard Deviation 0.30g/dL
Cu SerumOnce a Day Trientine0.54Standard Deviation 0.30mcg/24h
Cu SerumOnce a Day Trientine0.52Standard Deviation 0.30mcg/24h
Cu UrineOnce a Day Trientine287.9Standard Deviation 259.1mcg/24hr
Cu UrineOnce a Day Trientine313.4Standard Deviation 191.7mcg/24hr

Participant flow3

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

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDOnce a Day Trientine8
Overall StudyCOMPLETEDOnce a Day Trientine8
Overall StudyNOT COMPLETEDOnce a Day Trientine0

Adverse events0

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

None in this release.

Adverse event totals3

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityOnce a Day Trientine
Total, other adverse eventsOnce a Day Trientine08
Total, serious adverse eventsOnce a Day Trientine08

Papers11

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource
3600712BACKGROUNDPubMed
6121964BACKGROUNDPubMed
8119682BACKGROUNDPubMed
11241029BACKGROUNDPubMed
11602847BACKGROUNDPubMed
12774027BACKGROUNDPubMed
12955875BACKGROUNDPubMed
14713890BACKGROUNDPubMed
16233999BACKGROUNDPubMed
16606763BACKGROUNDPubMed

1 to 10 of 11

See all 11 papers

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/NCT01472874

GET https://conductscience.org/api/trials/v1/NCT01472874/registered