Ignite Creation Date:
2024-05-06 @ 7:08 AM
Last Modification Date:
2024-10-26 @ 11:45 AM
Study NCT ID:
NCT02477605
Status:
COMPLETED
Last Update Posted:
2018-07-02
First Post:
2015-06-18
Brief Title:
Clinical Comparison of 27 and 23-gauge ULTRAVIT 7500 Cpm Vitrectomy Outcomes
Sponsor:
Alcon Research
Organization:
Alcon Research
Study Overview
Official Title:
Clinical Comparison of 27 and 23-gauge ULTRAVIT 7500 Cpm Vitrectomy Outcomes
Status:
COMPLETED
Status Verified Date:
2017-06
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
The purpose of this study is to compare the treatment day change between immediate postoperative and immediate preoperative intraocular pressure IOP between 27-gauge and 23-gauge vitrectomy instruments
Detailed Description:
Required follow-up for this study is 3 months post treatment
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
True
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
False
Is an FDA AA801 Violation?:
None