Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
Healthy Volunteers
ID06694051

Application of Phototherapeutic Keratectomy Mode to Mark the Axis of Astigmatism

Led by Tianjin Eye Hospital · Updated on 2024-11-19

100

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

This research aims to improve correction of astigmatism during corneal refractive surgery by using phototherapeutic keratectomy (PTK) mode to precisely mark the axis of astigmatism. Astigmatism correction is challenging because it involves both magnitude and direction, and errors can occur due to head or eye rotation. The study explores using excimer laser therapeutic keratectomy to set laser parameters for accurate axis marking, aided by static cyclotorsion of the eye. Participants will be divided into two groups: one receiving the PTK mode marking procedure (experimental group) and one with no intervention (limbus group). The PTK mode aims to precisely mark the astigmatism axis using laser treatment. The study is non-randomized and open-label, with no masking. No additional treatments or procedures beyond the marking are described. During the study, researchers will measure participants' eye refraction three months after the procedure to assess the accuracy of astigmatism correction. Participants must be at least 18 years old and free of ocular diseases. The trial also allows healthy volunteers. The total duration and follow-up details focus mainly on the primary outcome at three months post-treatment.

CONDITIONS

Brief Title

Application of Phototherapeutic Keratectomy Mode to Mark the Axis of Astigmatism

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • At least 18 years old
Not Eligible

You will not qualify if you...

  • Presence of any ocular disease or eye condition

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - Single procedure with follow-up to 3 months

Participants receive axis marking using the phototherapeutic keratectomy mode or no intervention depending on group assignment.

1 treatment visit and follow-up visits over 3 months

Trial Site Locations

Total: 1 location

1

Tianjin Eye Hospital

Tianjin, Tianjin Municipality, China, 300020

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Research Team

W

Wang

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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