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Clinical Trials/NCT02055378
NCT02055378CompletedNot Applicable

the Effect of Low-Concentration Atropine Combined With Auricular Acupoint Stimulation in Myopia Control

Taipei Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation1 site in 1 country73 target enrollmentStarted: January 2011Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
73
Locations
1
Primary Endpoint
the change in spherical equivalent (SE)

Study Overview

Brief Summary

To compare the effect of myopia control between patients treated with low-concentration atropine eye drops combined with auricular acupoint stimulation and those treated with atropine alone.

Detailed Description

Myopia has been an increasing problem among school children, especially in Asian countries. High myopia is not only a refractive problem, but also a disease that can result in a number of sight-threatening complications such as macular degeneration, retinal detachment, glaucoma, and cataract. Atropine is a long-acting non-selective muscarinic antagonist that blocks accommodation by paralyzing ciliary muscles; it may affect remodeling of the sclera and suppress the elongation of axial length. Acupuncture and acupressure have been widely used in traditional Chinese medicine for thousands of years. Auricular acupoint stimulation by acupuncture or acupressure has been reported to improve visual acuity in myopic patients. Therefore, we want to compare the effect of myopia control between patients treated with low-concentration atropine eye drops combined with auricular acupoint stimulation and those who treated with atropine alone.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Care Provider)

Eligibility Criteria

Ages
6 Years to 12 Years (Child)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Children aged from 6 to 12 years with myopia, defined as spherical equivalent (SE) of -0.5 diopter (D) or less, were recruited from the outpatient clinics from January 2011 to June 2012.

Exclusion Criteria

  • (1) abnormal IOP (>21 mmHg) at presentation, (2) astigmatism or anisometropia of more than 1.5 D, (3) amblyopia or strabismus, (4) the presence of any related eyelid diseases, ocular diseases, or auricular diseases, (5) the presence of hemostatic disorders or other related major systemic diseases, (6) history of allergy to atropine, (7) previous or current use of contact lenses, bifocals, progressive lenses, or other forms of treatment for myopia.

Arms & Interventions

auricular acupoint stimulation

Experimental

Five auricular acupoints were selected for taping stimulation by using a 1-mm alloy ball by fingers three times a day, each time for five minutes over the five selected acupoints. Topical 0.125% atropine was given nightly.

Intervention: Atropine (Drug)

auricular acupoint stimulation

Experimental

Five auricular acupoints were selected for taping stimulation by using a 1-mm alloy ball by fingers three times a day, each time for five minutes over the five selected acupoints. Topical 0.125% atropine was given nightly.

Intervention: auricular acupoint stimulation (Device)

Atropine

Active Comparator

topical 0.125% atropine was given nightly during the study period.

Intervention: Atropine (Drug)

Outcomes

Primary Outcomes

the change in spherical equivalent (SE)

Time Frame: SE measured at 3, 6, 9, 12 months.

We measured the myopic progression (change in SE) of all the participants for at least six months.

Secondary Outcomes

  • axial length (AL) elongation, anterior chamber depth (ACD) and intraocular pressure(IOP)(AL, ACD, and IOP measure at 3, 6, 9, 12 months)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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