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Trial · NCT00762645

Travoprost 0.004% Versus Pilocarpine 1% in Patients With Chronic Angle Closure Glaucoma (CACG)

NCT00762645, Phase 4, Completed, Alcon Research; results first posted 2010-03-15

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Travoprost 0.004% Versus Pilocarpine 1% in Patients With Chronic Angle Closure Glaucoma (CACG). Trials, record NCT00762645. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT00762645

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Trial

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

Title
Travoprost 0.004% Versus Pilocarpine 1% in Patients With Chronic Angle Closure Glaucoma (CACG)
NCT number
NCT00762645
Status
Completed
Phases
Phase 4
Enrollment
30 participants, actual
Lead sponsor
Alcon Research
Conditions
Angle-closure Glaucoma
Interventions
Travoprost 0.004% (Travatan), Pilocarpine 1%
First posted
2008-09-30
Last updated
2023-12-06
Results first posted
2010-03-15

Source ClinicalTrials.gov

Registered outcomes2

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

ListOutcomeTime frameDescription
PrimaryMean Intraocular Pressure (IOP)4PM at Week 12 Visit
SecondaryNumber of Patients With Peripheral Anterior Synechiae (PAS)Week 12 Visit

Outcomes2

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

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYMean Intraocular Pressure (IOP)4PM at Week 12 Visitmillimeters mercury (mm Hg)MEAN
SECONDARYNumber of Patients With Peripheral Anterior Synechiae (PAS)Week 12 VisitParticipantsNUMBER

Results by group4

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

OutcomeGroupCategoryValueSpreadUnits
Mean Intraocular Pressure (IOP)Travoprost 0.004% (Travatan)15.77Standard Deviation 2.32millimeters mercury (mm Hg)
Mean Intraocular Pressure (IOP)Pilocarpine 1%18.35Standard Deviation 3.72millimeters mercury (mm Hg)
Number of Patients With Peripheral Anterior Synechiae (PAS)Travoprost 0.004% (Travatan)0Participants
Number of Patients With Peripheral Anterior Synechiae (PAS)Pilocarpine 1%0Participants

Participant flow6

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

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDTravoprost 0.004% (Travatan)16
Overall StudySTARTEDPilocarpine 1%14
Overall StudyCOMPLETEDTravoprost 0.004% (Travatan)12
Overall StudyCOMPLETEDPilocarpine 1%12
Overall StudyNOT COMPLETEDTravoprost 0.004% (Travatan)4
Overall StudyNOT COMPLETEDPilocarpine 1%2

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 mortalityTravoprost 0.004% (Travatan)
Total, all-cause mortalityPilocarpine 1%
Total, other adverse eventsTravoprost 0.004% (Travatan)016
Total, other adverse eventsPilocarpine 1%014
Total, serious adverse eventsTravoprost 0.004% (Travatan)016
Total, serious adverse eventsPilocarpine 1%014

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 comparisons2

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

ComparisonSource
Travoprost 0.004% (Travatan) vs Pilocarpine 1%: Number of Patients With Peripheral Anterior Synechiae (PAS)Trial comparisons
Travoprost 0.004% (Travatan) vs Pilocarpine 1%: serious adverse eventsTrial comparisons

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/NCT00762645

GET https://conductscience.org/api/trials/v1/NCT00762645/registered