Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT04126174 · ClinicalTrials.gov registry record · NA
Femtosecond Laser-assisted Arcuate Incisions Versus Manual Arcuate Incisions Outcomes
A NA study, sponsored by Gainesville Eye Associates.
- Completed
- Registry status
- NA
- Development phase
- 41
- Enrollment target
NCT04126174: Completed NA study, sponsored by Gainesville Eye Associates.
NCT04126174 is a NA study that has completed, run by Gainesville Eye Associates. The registered enrollment target is 41 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT04126174, a NA study, has completed, sponsored by Gainesville Eye Associates.
- COMPLETED
- Registry status
- NA
- Development phase
- 41 participants
- Enrollment target
Study Summary
This study is designed to compare the effectiveness of LenSx laser arcuate relaxing incisions vs. manual (blade) arcuate relaxing incisions in patients with low, but significant, levels of astigmatism.
Primary Outcome
Residual refractive astigmatism measured in diopters
Interventions
- DEVICE femtosecond laser system arcuate corneal incision
- OTHER Manual LRI
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 41 participants |
| Start Date | 2019-10-15 |
| Est. Completion | 2021-03-20 |
| Phase | NA |
What the finished NCT04126174 record still lists
NCT04126174 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 41 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower).
The record links to 0 conditions, and to 2 interventions - of which femtosecond laser system arcuate corneal incision is the first listed.
NCT04126174 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT04126174 about?
NCT04126174 is a clinical study titled "Femtosecond Laser-assisted Arcuate Incisions Versus Manual Arcuate Incisions Outcomes". This study is designed to compare the effectiveness of LenSx laser arcuate relaxing incisions vs. manual (blade) arcuate relaxing incisions in patients with low, but significant, levels of astigmatism.
What is the current status of trial NCT04126174?
This trial is currently completed. It is a NA study. The enrollment target is 41 participants. The study started on 2019-10-15. Estimated completion is 2021-03-20.
What interventions are being tested in trial NCT04126174?
The interventions under investigation include: femtosecond laser system arcuate corneal incision (DEVICE), Manual LRI (OTHER).
Who is sponsoring clinical trial NCT04126174?
This trial is sponsored by Gainesville Eye Associates, which has 9 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT04126174's enrollment target sits among peer trials
41 1446th of 2000 higher than 554 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
Nationwide trials with similar profiles
Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.
Similar enrollment target
- NCT03449238 · 41 participants · Phase 1
Pembrolizumab And Stereotactic Radiosurgery (Srs) Of Selected Brain Metastases In Breast Cancer Patients
- NCT03900793 · 41 participants · Phase 1
Losartan + Sunitinib in Treatment of Osteosarcoma
- NCT04082520 · 41 participants · Phase 2
Lutathera for the Treatment of Inoperable, Progressive Meningioma After External Beam Radiation Therapy
- NCT04220190 · 41 participants · Phase 2
RAPA-501 Therapy for ALS
Similar registry start date
- NCT05962346 · started 2026-12 · NA
Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia
- NCT07125183 · started 2026-12 · Phase 2
Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma
- NCT07292298 · started 2026-11 · Phase 2
Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates
- NCT04263285 · started 2026-10 · NA
Treatment of Depression Post-SCI