Clinical Trials Directory

Trials / Completed

CompletedNCT00457717

Myopia Control by Combining Auricular Acupoint and Atropine Eyedrops

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
60 (planned)
Sponsor
China Medical University, China · Academic / Other
Sex
All
Age
6 Years – 15 Years
Healthy volunteers
Not accepted

Summary

This study was designed to compare the difference of using atropine eyedrops alone from atropine combined with the stimulation of auricular acupoints therapy in reducing myopia progression.

Detailed description

A total of 64 school-aged children with myopia, fulfilling eligibility criteria, were recruited. They were randomly assigned to three arms: 1. 21 treated with the 0.25 % atropine each night (0.25A). 2. 20 treated with the 0.5 % atropine each night (0.5A). 3. 23 treated with 0.25 % atropine each night together with stimulation of auricular acupoints(0.25A+E). This protocol was proceeded for at least 6 months.The differences in post-treatment effects of these three groups were statistically accessed.

Conditions

Interventions

TypeNameDescription
DRUG0.25 % atropine
DRUG0.5 % atropine
PROCEDURE0.25 % atropine+auricular acupoints

Timeline

Start date
2005-07-01
Completion
2006-07-01
First posted
2007-04-06
Last updated
2007-04-06

Locations

1 site across 1 country: Taiwan

Source: ClinicalTrials.gov record NCT00457717. Inclusion in this directory is not an endorsement.