Viewing Study NCT05202808


Ignite Creation Date: 2025-12-26 @ 10:56 AM
Ignite Modification Date: 2026-01-01 @ 6:32 AM
Study NCT ID: NCT05202808
Status: COMPLETED
Last Update Posted: 2025-04-20
First Post: 2021-12-29
Is NOT Gene Therapy: True
Has Adverse Events: True

Brief Title: RxSight Light Adjustable Lens and Light Delivery Device New Enrollment Study
Sponsor: RxSight, Inc.
Organization:

Study Overview

Official Title: RxSight Light Adjustable Lens (LAL) And Light Delivery Device (LDD) New Enrollment Study
Status: COMPLETED
Status Verified Date: 2025-04
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 primary objective of this study is to conduct a post-approval study which compares the LAL to a monofocal control IOL for safety outcomes.
Detailed Description: None

Study Oversight

Has Oversight DMC: False
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?: