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Trial · NCT00206323

A Randomized, Placebo-controlled, Tourette Syndrome Study.

NCT00206323, Phase 3, Completed, Baylor College of Medicine; results first posted 2017-11-06

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. A Randomized, Placebo-controlled, Tourette Syndrome Study. Trials, record NCT00206323. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT00206323

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Trial

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

Title
A Randomized, Placebo-controlled, Tourette Syndrome Study.
NCT number
NCT00206323
Status
Completed
Phases
Phase 3
Enrollment
29 participants, actual
Lead sponsor
Baylor College of Medicine
Conditions
Tourette Syndrome
Interventions
Topiramate (drug), placebo/sugar pill
First posted
2005-09-21
Last updated
2020-02-12
Results first posted
2017-11-06

Source ClinicalTrials.gov

Registered outcomes1

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

ListOutcomeTime frameDescription
PrimaryChange From Baseline in Total Tic Score at Day 70baseline and Day 70
A component of the Yale Global Tic Severity Scale (YGTSS), the change from baseline in Total Tic Score (TTS) at visit 5 (day 70) is the pre-defined primary endpoint. The Total Tic Score (TTS) is a summation of the Total Motor Tic and Total Phonic Tic Scores. The Overall Impairment Rating is rated on a 50-point scale anchored by 0 (No impairment) and 50 (Severe impairment).

Outcomes1

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

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYChange From Baseline in Total Tic Score at Day 70baseline and Day 70units on a scaleMEAN

Results by group2

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

OutcomeGroupCategoryValueSpreadUnits
Change From Baseline in Total Tic Score at Day 70Placebo/Sugar Pill-5.0Standard Deviation 9.88units on a scale
Change From Baseline in Total Tic Score at Day 70Topiramate-14.29Standard Deviation 10.47units on a scale

Participant flow6

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

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDPlacebo/Sugar Pill14
Overall StudySTARTEDTopiramate15
Overall StudyCOMPLETEDPlacebo/Sugar Pill8
Overall StudyCOMPLETEDTopiramate12
Overall StudyNOT COMPLETEDPlacebo/Sugar Pill6
Overall StudyNOT COMPLETEDTopiramate3

Adverse events12

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

TypeEventOrgan systemGroupAffectedAt riskEvents
otherheadacheGeneral disordersPlacebo/Sugar Pill3143
otherheadacheGeneral disordersTopiramate3153
otherdiarrheaGastrointestinal disordersPlacebo/Sugar Pill1141
otherdiarrheaGastrointestinal disordersTopiramate3153
otherabdominal painGastrointestinal disordersPlacebo/Sugar Pill2142
otherabdominal painGastrointestinal disordersTopiramate2152
otherdrowsinessGeneral disordersPlacebo/Sugar Pill2142
otherdrowsinessGeneral disordersTopiramate2152
othercognitive slowingGeneral disordersPlacebo/Sugar Pill0140
othercognitive slowingGeneral disordersTopiramate1151

Adverse event totals6

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityPlacebo/Sugar Pill
Total, all-cause mortalityTopiramate
Total, other adverse eventsPlacebo/Sugar Pill814
Total, other adverse eventsTopiramate1115
Total, serious adverse eventsPlacebo/Sugar Pill014
Total, serious adverse eventsTopiramate015

Papers1

The papers the trial lists on ClinicalTrials.gov.

PMIDListed as
19726418BACKGROUND

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 comparisons1

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

Comparison
Topiramate vs Placebo/Sugar Pill: 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/NCT00206323

GET https://conductscience.org/api/trials/v1/NCT00206323/registered