Trials / Completed
CompletedNCT03247751
Evaluation of the Rotational Stability
Rotational Stability of the Blue Light-absorbing Hydrophobic Acrylic Posterior Chamber Single Piece Intraocular Lens
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 95 (actual)
- Sponsor
- Nidek Co. LTD. · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
To evaluate rotational stability of the investigational device implanted after cataract surgery.
Detailed description
The primary endpoint is angle of intraocular lens rotation between the day of surgery and postoperative 6 months.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | intraocular lens | Implant NIDEK intraocular lens after cataract surgery |
Timeline
- Start date
- 2016-06-01
- Primary completion
- 2017-08-01
- Completion
- 2017-11-01
- First posted
- 2017-08-14
- Last updated
- 2023-06-07
Source: ClinicalTrials.gov record NCT03247751. Inclusion in this directory is not an endorsement.