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Trial · NCT02909140

Outcomes12

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

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYPupil Size Immediately Prior to CapsulorrhexisImmediately prior to the capsulorrhexis step of cataract surgeryData was only collected for the Intracameral Mydriasis' arm. We analyzed data for 1 participant only because of lack of data for the other participant.mmNUMBER
SECONDARYPupil Size (mm) Immediately After Nuclear DisassemblyImmediately after nuclear disassembly step of cataract surgeryData was only collected for the Intracameral Mydriasis' arm. We analyzed data for 1 participant only because of lack of data for the other participant.mmNUMBER
SECONDARYPupil Size Immediately Prior to Intraocular Lens (IOL) InsertionImmediately prior to IOL insertion step of cataract surgeryData was only collected for the Intracameral Mydriasis' arm. We analyzed data for 1 participant only because of lack of data for the other participant.mmNUMBER
SECONDARYPupil Size Upon Completion of SurgeryintraoperativeData was only collected for the Intracameral Mydriasis' arm. We analyzed data for 1 participant only because of lack of data for the other participant.mmNUMBER
SECONDARYPupil Size on Post-operative Day 1Post-operative Day 1Data not available because it wasn't collected
SECONDARYPercentage of Patients in Each Arm That Required Another Mydriatic AgentintraoperativeData was only collected for the Intracameral Mydriasis' armpercent of participantsNUMBER
SECONDARYCumulative Energy Dispersed for Each ArmDuring cataract surgeryData was only collected for the Intracameral Mydriasis' arm. We analyzed data for 1 participant only because of lack of data for the other participant.Percent-secondsNUMBER
SECONDARYMean Time Taken to Perform Phacoemulsification in Each ArmintraoperativeData was only collected for the Intracameral Mydriasis' arm. We analyzed data for 1 participant only because of lack of data for the other participant.secondsNUMBER
SECONDARYPercentage of Patients With an Increase in the Blood Pressure or Heart RateBaselineData not available because data was not collected
SECONDARYPercentage of Patients With an Increase in the Blood Pressure or Heart RateintraoperativeData not available because data was not collected
SECONDARYMean Time Taken to Perform PhacoemulsificationDuring cataract surgeryData was only collected for the Intracameral Mydriasis' arm We analyzed data for 1 participant only because of lack of data for the other participant.secondsNUMBER
SECONDARYPercentage of Patients in Each Arm That Required Use of an Iris Expansion Device During the ProcedureintraoperativeData was only collected for the Intracameral Mydriasis' armpercentNUMBER

Source ClinicalTrials.govtrials-2026-11-12-0.5.0

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.

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