At a glance
ClinicalIndex Comparison RecordN/ACompleted· 38 enrolled
Drug / intervention
B&L Investigational Contact Lensdevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
The Study to Evaluate the Product Performance of a New Silicone Hydrogel Contact Lens
In Brief
A clinical study evaluating B&L Investigational Contact Lens for Corneal Deformity. Completed, enrolled 38 participants across 1 site.
Detailed Summary
This will be a randomized non-dispensing study comparing the overnight corneal swelling of an eye while wearing no contact lens to the Ultra contract lens.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsCorneal Deformity
CountriesUnited States
Collaborators--
Timeline
N/ACompletedFinished
201520162017201820192020202120222023202420252026
First PostedOct 2014
Enrollment StartNov 2014
Primary CompletionDec 2014
TodayJul 2026
First PostedOct 7, 2014
Enrollment StartNov 3, 2014
Primary CompletionDec 11, 2014
TodayJul 2, 2026
Enrollment to primary: 1 monthPosted 11.7 years ago
Interventions
B&L Investigational Contact Lensdevice
The lens used in this study will be supplied by the Sponsor. All subjects will wear a -3.00D lens.