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Clinical Eye Trials & Ophthalmology Research

Current Clinical Trials

General Study Guidelines:

  • Most studies require the participant to be 18+ years old
  • Cannot be pregnant or breastfeeding
  • Willing and able to complete all study visits
  • Reasonable travel expenses for some studies/visits may be approved
  • Complete visit schedules (including dates and times) are provided upon successful entry into any study
  • Visits can be rescheduled as required

Cataracts (Inflammation associated with post cataract surgery)

Clinical Trial Information

Condition Information

Patients must have inflammation and pain associated with cataract surgery

Inclusion Criteria

  • Subjects who are candidates for routine, uncomplicated unilateral cataract surgery

Length of Trial: 6 visits over 1 month

Study Stipend: $450.00 (upon successful completion of all visits)

Myopia in Children

Clinical Trial Information

Condition Information

Myopia, or nearsightedness, is defined as having a refractive error of worse than 0.50 diopters (-0.50 D).

Myopia is among the 5 conditions that have been identified as immediate priorities by the World Health Organization in its Global Initiative for the Elimination of Avoidable Blindness.

Inclusion Criteria

  • 3-14 years of age (at the time of screening)
  • Subject (or parent/guardian) has demonstrated ability to administer eyedrops
  • Myopia of 0.5 D to 6.00 D
    • Astigmatism ≤1.50 D
    • Anisometropia ≤1.00 D

Length of Trial: 11 visits over 4 years

Study Stipend: Up to $1152.00 (upon successful completion of all study visits and questionnaires) 

  • Reimbursements for new glasses/contact prescription changes may be provided (once per year).

Neovascular Age-related Macular Degeneration (Wet AMD)

Clinical Trial Information

Condition Information

Neovascular age-related macular degeneration is a medical condition which may result in blurred or no vision in the center of the visual field. Over time, however, some people experience a gradual worsening of vision that may affect one or both eyes.

Inclusion Criteria: 

  • Males and females 50 years of age and older
  • Diagnosis in the 12 weeks to 18 months prior to screening; treated with at least prior IVT injections of an anti-VEGF agent (aflibercept, bevacizumab, or
  • Additional criteria to be evaluated by Investigator.

Length of Trial: 15 visits over 13 months

Study Stipend: $125.00/visit for a total payment of up to $1,875.00 upon completion of all study visits.

Open Angle Glaucoma or Ocular Hypertension

Clinical Trial Information

Condition Information

Glaucoma is a collection of disorders characterized by a gradual loss of vision with several recognized risk factors, including increased intraocular pressure (IOP).

Inclusion Criteria

  • Have open angle glaucoma, or ocular hypertension in both eyes and likely to be controlled on monotherapy.
  • Unmedicated intraocular pressure (IOP) ≥ 22 mmHg and ≤ 34 mmHg in at least one eye

Length of Trial: 5 visits over 3 months

Study Stipend: $500.00 (upon successful completion of all visits)


Clinical Trial Information

Condition Information

Uveitis is inflammation of the middle layer of the eye. It is sometimes caused by an eye injury or sometimes a disease elsewhere in the body.

Inclusion Criteria

  • Must have active moderate to severe Uveitis.
  • Additional criteria to be evaluated by an Investigator at Screening.

Length of Trial: 13 visits over 1 year

Contact one of our team members below or use the link to book an appointment

Kristen N. Peterson

Chief Operating Officer

Erica Glaser

Clinical Study Manager | 701.478.0061

Lance Bergstrom, MD

President / Principal Investigator

Carrie Iverson

Clinical Study Manager


At Bergstrom Eye and Laser Clinic, our goal is to provide the highest quality of care in a compassionate and ethical manner. We believe that vision is one of our most precious gifts.