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Trial · NCT00896779

Lucentis in Advanced Macular Degeneration

NCT00896779, Phase 2, Completed, Steven R. Sanislo; results first posted 2015-05-27

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Lucentis in Advanced Macular Degeneration. Trials, record NCT00896779. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT00896779

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Trial

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

Title
Lucentis in Advanced Macular Degeneration
NCT number
NCT00896779
Status
Completed
Phases
Phase 2
Enrollment
20 participants, actual
Lead sponsor
Steven R. Sanislo
Conditions
Macular Degeneration
Interventions
ranibizumab
First posted
2009-05-12
Last updated
2015-06-29
Results first posted
2015-05-27
Limitations and caveats
Limitations include small number of subjects analyzed and no control group that were untreated.

Source ClinicalTrials.gov

Registered outcomes1

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

ListOutcomeTime frameDescription
PrimaryMean Change in Visual Acuity12 months
Change in vision from baseline measurement at 12 months. Standard ETDRS chart (80 letters) was used to determine visual acuity with test luminance of 45 cd/m \^2 at 8 feet. Number of correctly read letters were reported.

Outcomes1

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

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYMean Change in Visual Acuity12 monthslettersMEAN

Results by group2

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

OutcomeGroupCategoryValueSpreadUnits
Mean Change in Visual AcuityRanibizumab Group 115.0Standard Deviation 14.2letters
Mean Change in Visual AcuityRanibizumab Group 25.6Standard Deviation 8.6letters

Participant flow6

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

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDRanibizumab Group 18
Overall StudySTARTEDRanibizumab Group 212
Overall StudyCOMPLETEDRanibizumab Group 18
Overall StudyCOMPLETEDRanibizumab Group 211
Overall StudyNOT COMPLETEDRanibizumab Group 10
Overall StudyNOT COMPLETEDRanibizumab Group 21

Adverse events38

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

TypeEventOrgan systemGroupAffectedAt riskEvents
otherlaceration right legSkin and subcutaneous tissue disordersRanibizumab Group 118
otherlaceration right legSkin and subcutaneous tissue disordersRanibizumab Group 2012
otherlaceration left legSkin and subcutaneous tissue disordersRanibizumab Group 118
otherlaceration left legSkin and subcutaneous tissue disordersRanibizumab Group 2012
otherMild pneumoniaRespiratory, thoracic and mediastinal disordersRanibizumab Group 118
otherMild pneumoniaRespiratory, thoracic and mediastinal disordersRanibizumab Group 2012
otherSeasonal allergiesImmune system disordersRanibizumab Group 118
otherSeasonal allergiesImmune system disordersRanibizumab Group 2012
otherWorsening glaucoma - which eye was not specifiedEye disordersRanibizumab Group 118
otherWorsening glaucoma - which eye was not specifiedEye disordersRanibizumab Group 2012

Adverse event totals6

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityRanibizumab Group 1
Total, all-cause mortalityRanibizumab Group 2
Total, other adverse eventsRanibizumab Group 148
Total, other adverse eventsRanibizumab Group 2412
Total, serious adverse eventsRanibizumab Group 108
Total, serious adverse eventsRanibizumab Group 2012

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
Ranibizumab Group 1 vs Ranibizumab Group 2: 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/NCT00896779

GET https://conductscience.org/api/trials/v1/NCT00896779/events?page=2