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NCT04533191 · ClinicalTrials.gov registry record
Binocular Custom Vision Utilizing The Light Adjustable Lens (LAL)
A clinical trial of Cataract and Pseudophakia, sponsored by Vance Thompson Vision.
- Completed
- Registry status
- 25
- Enrollment target
- 1
- Study location
NCT04533191 is a study of Cataract and Pseudophakia that has completed, run by Vance Thompson Vision. The registered enrollment target is 25 participants, below the 228-participant average among 83 other Cataract trials with a reported enrollment target (89% lower). The trial reports 1 study location across 1 state.
The verdict
NCT04533191, a study of Cataract and Pseudophakia, has completed, sponsored by Vance Thompson Vision.
- COMPLETED
- Registry status
- 25 participants
- Enrollment target
- 1
- Study location
Study Summary
The objective of this investigator initiated study (IIT-001) is to obtain data on clinical methods which can be used during the examination of patients desiring binocular custom vision with the Light Adjustable Lens (LAL). An analysis of the collected data will be performed to determine whether these clinical assessments can be used by doctors to enhance their patient's clinical outcome.
Conditions Studied
Interventions
- PROCEDURE LAL IOL lens
Study Locations (1)
South Dakota
- Vance Thompson Vision - Sioux Falls
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 25 participants |
| Start Date | 2020-09-01 |
| Est. Completion | 2021-02-01 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT04533191
The ClinicalTrials.gov registry entry for NCT04533191 describes a study currently listed as completed, categorized as an unspecified phase. The registered enrollment target is 25 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 228-participant average among 83 other Cataract trials with a reported enrollment target (89% lower). The listed sponsor is Vance Thompson Vision, which has 14 total studies on file at ClinicalTrials.gov.
The record links to 2 conditions, with Cataract appearing as the primary indexed condition, and to 1 intervention - of which LAL IOL lens is the first listed.
NCT04533191 reports 1 study location spanning 1 distinct geographic area - top geographies include South Dakota.
Frequently Asked Questions
What is clinical trial NCT04533191 about?
NCT04533191 is a clinical study titled "Binocular Custom Vision Utilizing The Light Adjustable Lens (LAL)". The objective of this investigator initiated study (IIT-001) is to obtain data on clinical methods which can be used during the examination of patients desiring binocular custom vision with the Light Adjustable Lens (LAL). An analysis of the collected data will be performed to determine whether thes...
What is the current status of trial NCT04533191?
This trial is currently completed. The enrollment target is 25 participants. The study started on 2020-09-01. Estimated completion is 2021-02-01.
What conditions does trial NCT04533191 study?
This clinical trial studies the following conditions: Cataract, Pseudophakia.
What interventions are being tested in trial NCT04533191?
The interventions under investigation include: LAL IOL lens (PROCEDURE).
Who is sponsoring clinical trial NCT04533191?
This trial is sponsored by Vance Thompson Vision, which has 14 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT04533191 being conducted?
This trial has 1 study location across South Dakota. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Read our methodology - how this data is sourced, computed, and verified.
Related
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