Sioux Falls, SDNCT07790185Now EnrollingIRB Ready

Astigmatism Clinical Trial in Sioux Falls, SD

Access cutting-edge astigmatism treatment through this phase 4 clinical trial at a research site in Sioux Falls. Study-provided care at no cost to qualified participants.

Sponsored by Vance Thompson Vision

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Expert Care in Sioux Falls

Access astigmatism specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related astigmatism treatment provided free

Apply for This Sioux Falls Location

Check if you qualify for this astigmatism clinical trial in Sioux Falls, SD

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Your information is protected and will only be shared with the research team.

Why Participate?

  • No-Cost Study Care

  • Local to Sioux Falls

    Convenient for SD residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit Sioux Falls site if eligible
  4. 4Begin participation

About This Astigmatism Study in Sioux Falls

To provide comprehensive evaluation of WaveLight® Plus technology by assessing impact on both functional low-light vision and patient reported outcomes

Sponsor: Vance Thompson Vision

Who Can Participate

Inclusion Criteria

Subjects ages 18 to 45 years old.
Stable refraction (within ± 0.50 D) as determined by manifest refraction spherical equivalent for a minimum of 12 months prior to surgery or stability as determined by the investigator.
Myopia with or without astigmatism and MRSE within the range of indications for wavelight plus (myopia up to -8.00D, astigmatism up to -3.00D, S.E. more than -1.00 and up to -9.00D)
Best corrected distance visual acuity (BCDVA) of 20/20 or better (≥83 letters) in each eye.
Subjects who have elected to undergo bilateral LASIK targeted for emmetropia.
Subjects must be able and willing to return for scheduled follow-up examinations after surgery.
Subjects must be able to read, understand and provide written informed consent on the Institutional Review Board (IRB) approved Informed Consent Form (ICF) and provide authorization as appropriate for local privacy regulations.
Mesopic pupil size ≥4.5mm
Less than 0.75D spherical equivalent differences between Sightmap measured refraction SE and the subjective manifest refraction (MRSE)
Subjects who regularly drive at night and expect to continue night driving throughout the duration of the study, as determined by investigator assessment

Exclusion Criteria

Pregnant or nursing women, or those who plan to become pregnant over the course of this clinical study or have another condition with associated fluctuation of hormones that could lead to refractive changes.
Dry eye syndrome that is unable to be controlled with ocular lubricant(s) or medication(s) and which may confound study outcomes in the opinion of the Investigator.
Previous corneal ocular surgery
History of evidence of active or inactive corneal disease or retinal vascular disease, keratoconus or glaucoma or glaucoma suspect.
Serious acute, chronic, or systemic, non-ophthalmic disease or illness that would increase the operative risk, confound the outcome(s) of the study or which may preclude study completion (e.g., immunocompromised, connective tissue disease, clinically significant atopic disease, uncontrolled diabetes, etc.), in the opinion of the Investigator.
Ocular condition (other than high myopia) that may predispose the subject to future complications, in the opinion of the Investigator.
Subjects who, in the judgment of the Investigator, present any emotional, physiological, or anatomical condition which may preclude participation in this study or provide an inappropriate landscape for the intended study treatment.
Patients with a calculated residual stromal depth \<250 um

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Sioux Falls?

Yes, this clinical trial (NCT07790185) has an active research site in Sioux Falls, SD that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Astigmatism Treatment Options in Sioux Falls, SD

If you're searching for astigmatism treatment options in Sioux Falls, SD, this clinical trial (NCT07790185) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Sioux Falls research site is actively enrolling participants for this phase 4 clinical trial. You'll receive care from experienced astigmatism specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all astigmatism clinical trials near you to find additional studies recruiting in your area.

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