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Trial · NCT00928954

Cross-over Comparison of Gabapentin and Memantine as Treatment for Acquired Nystagmus

NCT00928954, Not applicable, Completed, Case Western Reserve University; results first posted 2016-07-29

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Cross-over Comparison of Gabapentin and Memantine as Treatment for Acquired Nystagmus. Trials, record NCT00928954. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT00928954

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Trial

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

Title
Cross-over Comparison of Gabapentin and Memantine as Treatment for Acquired Nystagmus
NCT number
NCT00928954
Status
Completed
Phases
Not applicable
Enrollment
10 participants, actual
Lead sponsor
Case Western Reserve University
Conditions
Nystagmus
Interventions
gabapentin, memantine
First posted
2009-06-26
Last updated
2016-07-29
Results first posted
2016-07-29

Source ClinicalTrials.gov

Registered outcomes2

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

ListOutcomeTime frameDescription
PrimaryChange in logMAR Visual Acuity of Each Eye, Measured During Far or Near ViewingAfter 2 weeks of therapy, for both drugs
PrimaryPercent Change in Median Eye SpeedAfter 2 weeks of therapy, for both drugsMedian eye speed during attempted visual fixation by each eye

Outcomes2

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

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYChange in logMAR Visual Acuity of Each Eye, Measured During Far or Near ViewingAfter 2 weeks of therapy, for both drugslogMARNUMBER
PRIMARYPercent Change in Median Eye SpeedAfter 2 weeks of therapy, for both drugsPercent changeNUMBER

Results by group80

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

OutcomeGroupCategoryValueSpreadUnits
Change in logMAR Visual Acuity of Each Eye, Measured During Far or Near ViewingGabapentinParticipant 1, Right Eye0logMAR
Change in logMAR Visual Acuity of Each Eye, Measured During Far or Near ViewingMemantineParticipant 1, Right Eye0.1logMAR
Change in logMAR Visual Acuity of Each Eye, Measured During Far or Near ViewingGabapentinParticipant 1, Left Eye0.2logMAR
Change in logMAR Visual Acuity of Each Eye, Measured During Far or Near ViewingMemantineParticipant 1, Left Eye0.2logMAR
Change in logMAR Visual Acuity of Each Eye, Measured During Far or Near ViewingGabapentinParticipant 2, Right Eye0.1logMAR
Change in logMAR Visual Acuity of Each Eye, Measured During Far or Near ViewingMemantineParticipant 2, Right Eye0.2logMAR
Change in logMAR Visual Acuity of Each Eye, Measured During Far or Near ViewingGabapentinParticipant 2, Left Eye0.2logMAR
Change in logMAR Visual Acuity of Each Eye, Measured During Far or Near ViewingMemantineParticipant 2, Left Eye0logMAR
Change in logMAR Visual Acuity of Each Eye, Measured During Far or Near ViewingGabapentinParticipant 3, RIght Eye-0.1logMAR
Change in logMAR Visual Acuity of Each Eye, Measured During Far or Near ViewingMemantineParticipant 3, RIght Eye-0.2logMAR

Participant flow6

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

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDGabapentin First and Then Memantine4
Overall StudySTARTEDMemantine First, Then Gabapentin6
Overall StudyCOMPLETEDGabapentin First and Then Memantine4
Overall StudyCOMPLETEDMemantine First, Then Gabapentin6
Overall StudyNOT COMPLETEDGabapentin First and Then Memantine0
Overall StudyNOT COMPLETEDMemantine First, Then Gabapentin0

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 totals6

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityGabapentin
Total, all-cause mortalityMemantine
Total, other adverse eventsGabapentin010
Total, other adverse eventsMemantine010
Total, serious adverse eventsGabapentin010
Total, serious adverse eventsMemantine010

Papers0

The papers the trial lists on ClinicalTrials.gov.

None in this release.

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 comparisons1

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

Comparison
Gabapentin vs Memantine: serious adverse events

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/NCT00928954

GET https://conductscience.org/api/trials/v1/NCT00928954/results?page=2