Clinical Efficacy and Mechanism Exploration of MR-61 in Delaying the Progression of Myopia

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age3-18
SponsorSecond Affiliated Hospital of Nanchang University

About this trial

To investigate whether probiotic MR-61 can assist in slowing down the progression rate of myopia (a prospective randomized controlled study).

Eligibility criteria

Qualifiers

Myopia is defined as spherical equivalent (SE) ≤ -0.5D.

Aged between 3 and 18 years, with no restriction on gender.

Cylinder power ≤ 1.50D; anisometropia of SE between both eyes ≤ 1.50D.

The subject has sufficient compliance with the study follow-up; the subject or their guardian has the intention to receive treatment and has signed the informed consent form.

Disqualifiers

Presence of other concomitant ocular diseases;

Abnormal findings on clinical slit-lamp examination;

Existence of amblyopia, manifest strabismus, esotropia, or other congenital ocular diseases;

Individuals with abnormal intraocular pressure or abnormal axial length of the eye;

Trial design

Treatments tested in this trial

  • Investigational Bifidobacterium Preparation MR-61
  • Placebo for MR-61

Treatment groups

164 Participants
are divided into 2 treatment groups