Trials / Completed
CompletedNCT05011708
I-DROP MGD Symptomatic Relief and Tear Film Stability
Examining Symptomatic Relief and Kinetic Stability of I-DROP MGD Eye Drops (LIME)
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 10 (actual)
- Sponsor
- I-MED Pharma · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Accepted
Summary
The objective of the study is to compare the difference in tear film stability and symptomatic relief between I-DROP MGD and another commercially available drop in the Canadian market.
Detailed description
The purpose of this study is to: * Compare tear film measurements for two hours after putting one drop of I-DROP MGD eye drops into one eye and one drop of Thealoz Duo eye drops in the other eye. * Investigate the relief of dry eye symptoms with I-DROP MGD eye drops after 7 days of use.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | I-DROP MGD | I-DROP MGD are eye drop produced by I-MED PHARMA for the management of moderate to severe Dry Eye Disease. |
| DEVICE | Thealoz Duo | I-DROP MGD are eye drop produced by Laboratoires Thea for the management of Dry Eye Disease. |
Timeline
- Start date
- 2021-08-23
- Primary completion
- 2021-12-15
- Completion
- 2022-01-12
- First posted
- 2021-08-18
- Last updated
- 2022-03-29
Locations
2 sites across 1 country: Canada
Source: ClinicalTrials.gov record NCT05011708. Inclusion in this directory is not an endorsement.