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Trial · NCT01640171

Anesthesia Preference for Intravitreal Injection: Topical or Subconjunctival

NCT01640171, Not applicable, Completed, Retina Vitreous Associates of Florida; results first posted 2014-04-21

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Anesthesia Preference for Intravitreal Injection: Topical or Subconjunctival. Trials, record NCT01640171. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT01640171

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Trial

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

Title
Anesthesia Preference for Intravitreal Injection: Topical or Subconjunctival
NCT number
NCT01640171
Status
Completed
Phases
Not applicable
Enrollment
57 participants, actual
Lead sponsor
Retina Vitreous Associates of Florida
Conditions
Age-related Macular Degeneration, Central Retinal Vein Occlusion, Diabetic Macular Edema
Interventions
Xylocaine 2% Injectable Anesthetic, Proparacaine Hydrochloride 0.5% Drop, Tetravisc 0.5% Gel, Acuvail, Intra-vitreal Anti-VEGF Drug
First posted
2012-07-13
Last updated
2014-04-21
Results first posted
2014-04-21
Limitations and caveats
Most patients were treated with subconjunctival anesthetic prior to the study.

Source ClinicalTrials.gov

Registered outcomes3

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

ListOutcomeTime frameDescription
PrimaryNumber of Participants Who Preferred Subconjunctival Anesthetic at the Third Follow-up Visitup to 6 monthsParticipants received anesthetic over several treatment visits. They were allowed to change there preference at each visit. The final outcome was the preference indicated at the third follow-up visit.
SecondaryNumber of Participatns With Level 10 Pain on Wong-Baker Pain Scale In Subconjunctival Eye At Time of Intravitreal Injection24 hours
Pain was rated on a 10 point standardized pain scale, zero was the least pain and 10 was the worst pain. The patient was questioned using a script and shown a pain scale as well as told how the pain scale worked. Then the patient gave the number that characterized their pain.
SecondaryLikert Like Pain Scale Number of Participants Who Said the Topical Eye Hurt Much More Than the Subconjunctival Eye at Time of Intravitreal Injection24 hours
The patient was asked to compare the two eyes in the way described in the study protocol on a five point scale. If one eye hurt a lot more or a little more than the other or if the two eyes were equal (neither hurt more than the other).

Outcomes3

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

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYNumber of Participants Who Preferred Subconjunctival Anesthetic at the Third Follow-up Visitup to 6 monthsparticipantsNUMBER
SECONDARYNumber of Participatns With Level 10 Pain on Wong-Baker Pain Scale In Subconjunctival Eye At Time of Intravitreal Injection24 hoursAll patients in the studyparticipantsNUMBER
SECONDARYLikert Like Pain Scale Number of Participants Who Said the Topical Eye Hurt Much More Than the Subconjunctival Eye at Time of Intravitreal Injection24 hourstotal groupparticipantsNUMBER

Results by group3

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

OutcomeGroupCategoryValueSpreadUnits
Number of Participants Who Preferred Subconjunctival Anesthetic at the Third Follow-up VisitTopical Anesthesia 1 Eye, SC 1 Eye50participants
Number of Participatns With Level 10 Pain on Wong-Baker Pain Scale In Subconjunctival Eye At Time of Intravitreal InjectionTopical Anesthesia 1 Eye, SC 1 Eye0participants
Likert Like Pain Scale Number of Participants Who Said the Topical Eye Hurt Much More Than the Subconjunctival Eye at Time of Intravitreal InjectionTopical Anesthesia 1 Eye, SC 1 Eye19participants

Participant flow3

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

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDTopical Anesthesia 1 Eye, SC 1 Eye57
Overall StudyCOMPLETEDTopical Anesthesia 1 Eye, SC 1 Eye57
Overall StudyNOT COMPLETEDTopical Anesthesia 1 Eye, SC 1 Eye0

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 mortalityTopical Anesthesia
Total, all-cause mortalitySubconjunctival Anesthesia
Total, other adverse eventsTopical Anesthesia057
Total, other adverse eventsSubconjunctival Anesthesia057
Total, serious adverse eventsTopical Anesthesia057
Total, serious adverse eventsSubconjunctival Anesthesia057

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
Topical Anesthesia vs Subconjunctival Anesthesia: 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/NCT01640171

GET https://conductscience.org/api/trials/v1/NCT01640171/registered