Trial Outcomes & Findings for Dropless™ vs. Less Drops™ Pharmaceutical Regimens After Cataract Surgery (NCT NCT02819908)
NCT ID: NCT02819908
Last Updated: 2020-03-09
Results Overview
Based on Goldmann tonometry
COMPLETED
PHASE4
25 participants
To end of study (1 month postop)
2020-03-09
Participant Flow
Participant milestones
| Measure |
Imprimis Dropless
TriMoxiVanc 0.2cc intravitreal one time
Imprimis Dropless: Tri-Moxi-Vanc transzonular intravitreal injection
|
Imprimis Less Drops
Pred Moxi, 1 drop tid for 1 week then, PredKeterolac bid for 2-4 weeks.
Imprimis Less Drops: Pred-Moxi-Ketorolac and Pred-Ketorolac topical instillation qd postoperatively
|
|---|---|---|
|
Overall Study
STARTED
|
12
|
13
|
|
Overall Study
COMPLETED
|
12
|
13
|
|
Overall Study
NOT COMPLETED
|
0
|
0
|
Reasons for withdrawal
Withdrawal data not reported
Baseline Characteristics
Dropless™ vs. Less Drops™ Pharmaceutical Regimens After Cataract Surgery
Baseline characteristics by cohort
Baseline data not reported
PRIMARY outcome
Timeframe: To end of study (1 month postop)Population: Study data has been lost to natural disaster (Hurricane Micheal), therefore there is no study data that is available to report
Based on Goldmann tonometry
Outcome measures
Outcome data not reported
SECONDARY outcome
Timeframe: To end of study (1 month postop)Population: Study data has been lost to natural disaster (Hurricane Micheal), therefore there is no study data that is available to report
Based on corneal pachymetry
Outcome measures
Outcome data not reported
SECONDARY outcome
Timeframe: To end of study (1 month postop)Population: Study data has been lost to natural disaster (Hurricane Micheal), therefore there is no study data that is available to report
Outcome measures
Outcome data not reported
OTHER_PRE_SPECIFIED outcome
Timeframe: To end of study (1 month postop)Population: Study data has been lost to natural disaster (Hurricane Micheal), therefore there is no study data that is available to report
"0"( on the eye pain/discomfort scale)
Outcome measures
Outcome data not reported
OTHER_PRE_SPECIFIED outcome
Timeframe: To end of study (1 month postop)Population: Study data has been lost to natural disaster (Hurricane Micheal), therefore there is no study data that is available to report
eye pain/discomfort scale
Outcome measures
Outcome data not reported
OTHER_PRE_SPECIFIED outcome
Timeframe: To end of study (1 month postop)Population: Study data has been lost to natural disaster (Hurricane Micheal), therefore there is no study data that is available to report
visual symptom scale
Outcome measures
Outcome data not reported
OTHER_PRE_SPECIFIED outcome
Timeframe: To end of study (1 month postop)Population: Study data has been lost to natural disaster (Hurricane Micheal), therefore there is no study data that is available to report
visual symptom scale
Outcome measures
Outcome data not reported
OTHER_PRE_SPECIFIED outcome
Timeframe: To end of study (1 month postop)Population: Study data has been lost to natural disaster (Hurricane Micheal), therefore there is no study data that is available to report
corneal pachymetry
Outcome measures
Outcome data not reported
OTHER_PRE_SPECIFIED outcome
Timeframe: To end of study (1 month postop)Population: Study data has been lost to natural disaster (Hurricane Micheal), therefore there is no study data that is available to report
based on optical coherence tomography (OCT) measurement
Outcome measures
Outcome data not reported
Adverse Events
Imprimis Dropless
Imprimis Less Drops
Serious adverse events
Adverse event data not reported
Other adverse events
Adverse event data not reported
Additional Information
Results disclosure agreements
- Principal investigator is a sponsor employee
- Publication restrictions are in place