Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT07127757 · ClinicalTrials.gov registry record

Clinical Evaluation of WaveLight Plus LASIK

A clinical trial of Myopia and Astigmatism, sponsored by Laser Defined Vision.

Recruiting
Registry status
50
Enrollment target
1
Study location

NCT07127757: Recruiting study of Myopia and Astigmatism, sponsored by Laser Defined Vision.

NCT07127757 is a study of Myopia and Astigmatism that is actively recruiting participants, run by Laser Defined Vision. The registered enrollment target is 50 participants, below the 267-participant average among 90 other Myopia trials with a reported enrollment target (81% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT07127757, a study of Myopia and Astigmatism, is actively recruiting participants, sponsored by Laser Defined Vision.

RECRUITING
Registry status
50 participants
Enrollment target
1
Study location

Study Summary

This study is a single-site, single-arm, prospective, observational study of subject satisfaction, quality of vision, and quality of life after bilateral LASIK surgery. Subjects will be assessed up to 3 months post-operatively. Clinical evaluations will include refractive outcomes, visual acuity, and administration of the adapted PROWL and Low Luminance Questionnaire (LLQ-32) Questionnaire.

Conditions Studied

Interventions

  • DEVICE Wavelight Plus LASIK

Study Locations (1)

North Carolina

  • Laser Defined Vision - Greensboro

Trial Details

FieldValue
Enrollment Target 50 participants
Start Date 2025-08-28
Est. Completion 2026-09-01
Laser Defined Vision

2 total trials

What NCT07127757 shows while recruiting

NCT07127757 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 50 participants, a relatively small participant target, below the 267-participant average among 90 other Myopia trials with a reported enrollment target (81% lower).

The record links to 2 conditions, with Myopia appearing as the primary indexed condition, and to 1 intervention - of which Wavelight Plus LASIK is the first listed.

NCT07127757 reports a single indexed study location in North Carolina.

Frequently Asked Questions

What is clinical trial NCT07127757 about?

NCT07127757 is a clinical study titled "Clinical Evaluation of WaveLight Plus LASIK". This study is a single-site, single-arm, prospective, observational study of subject satisfaction, quality of vision, and quality of life after bilateral LASIK surgery. Subjects will be assessed up to 3 months post-operatively. Clinical evaluations will include refractive outcomes, visual acuity, an...

What is the current status of trial NCT07127757?

This trial is currently recruiting. The enrollment target is 50 participants. The study started on 2025-08-28. Estimated completion is 2026-09-01.

What conditions does trial NCT07127757 study?

This clinical trial studies the following conditions: Myopia, Astigmatism.

What interventions are being tested in trial NCT07127757?

The interventions under investigation include: Wavelight Plus LASIK (DEVICE).

Who is sponsoring clinical trial NCT07127757?

This trial is sponsored by Laser Defined Vision, which has 2 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT07127757 being conducted?

This trial has 1 study location across North Carolina. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Myopia

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT07127757's enrollment target sits among peer trials

50 70th of 90 higher than 16 of 90 other Myopia trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Myopia 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

  • NCT00200889 · 50 participants · Early Phase 1

    Mapping Auricular Vagus Nerve Circuitry

  • NCT00409435 · 50 participants · Phase 2

    A Study of Pyridostigmine in Postural Tachycardia Syndrome

  • NCT01202305 · 50 participants

    The Use of Lymph Node Biopsies to Support HIV Pathogenesis Studies

  • NCT01225913 · 50 participants · Phase 4

    Mechanism(s) of Airflow Limitation During Exacerbation of Asthma

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

Source: ClinicalTrials.gov NCT07127757, the US trial registry maintained by the National Library of Medicine. NCT07127757 (small enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.