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The Efficacy and Safety of Periocular Acupoint Stimulation on Myopia Progression in Children

K

Korean Medicine Hospital of Pusan National University

Status and phase

Completed
Phase 1

Conditions

Myopia

Treatments

Device: massager

Study type

Interventional

Funder types

Other

Identifiers

NCT02064660
blueicek

Details and patient eligibility

About

Myopia is widely one of the three commonly detected refractive errors. Myopia is usually managed by correction through glasses or contact lenses. Other alternative available include surgery, drugs and acupuncture. There are various therapeutic approaches and different points can be used in acupuncture treatment for myopia, such as auricular acupuncture, acupressure body acupuncture. However, the mechanism of acupuncture therapy for myopia is largely unknown. Furthermore, little information exists regarding the effects and safety of acupuncture for degenerative myopia in children.

The investigators aimed to assess the overall effectiveness, safety of periocular acupressure for children with myopia

The hypotheses of this study are as follows:

Periocular acupressure is effective for myopia progression delay.

The study aims to include 56 participants.

Enrollment

20 patients

Sex

All

Ages

7 to 12 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Aged 7-12 years
  • Spherical equivalent greater than -5D
  • Individuals without strabismus, anistopia
  • Willingness to participate in the study

Exclusion criteria

  • The presence of a related disease such as cataract, glaucoma, or other eye disease.
  • Individuals who were received ocular or scalp trauma.
  • Individuals who were received ocular surgery and had ocular wound.
  • Individuals who were adapted bifocal lense.
  • Individuals suffering fever or bad conditions.
  • Individuals suffering systemic or neurologic disease.
  • Indibiduals who were receiving other therapy during the period of study
  • Individuals who did not comply with the treatment which affected myopia progression.

Trial design

Primary purpose

Prevention

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

20 participants in 1 patient group

single arm
Experimental group
Description:
A series of acupressure sessions within six months from the baseline
Treatment:
Device: massager

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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