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A study of the effects of fascial release on the visual acuity of adolescents with pseudo and low myopia

Phase 1
Conditions
Video terminal visual fatigue, pseudo-myopia, low-level myopia
Registration Number
ITMCTR2200005698
Lead Sponsor
Guangzhou Medical University
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
All
Target Recruitment
Not specified
Inclusion Criteria

1. Aged 18-25 years, no gender limit;
2. Meet the VDT diagnostic criteria;
3. Those without organic lesions of the eyes and head;
4. Those who have not been treated or have been treated with other drugs for more than 2 weeks;
5. Proficient in the use of smart phones;
6. Those who signed the informed consent;
7. No history of head trauma or surgery.

Exclusion Criteria

1. Subjects with poor compliance;
2. Subjects with serious diseases (such as diabetes, liver and kidney disease and (or) heart disease, thyroid disease, adrenal disease);
3. Those with other eye diseases (such as infectious conjunctivitis, glaucoma);
4. Subjects diagnosed with presbyopia (the dominant eye's controlled width is less than 2.5 diopters (D));
5. Subjects with uncorrected severe refractive errors in the dominant eye;
6. Subjects who have undergone ophthalmic surgery;
7. Subjects whose dominant eye can achieve the best corrected visual acuity advantage <1.0;
8. Subjects with serious diseases (such as diabetes, liver disease, kidney disease and (or) heart disease, thyroid disease, adrenal disease);
9. Subjects who often take drugs or health food that may have an effect on the eyes or are expected to use related drugs or health food during the study period;
10. Subjects who may cause drug allergy;
11. Those who plan or have participated in other clinical studies during this study within 3 months.

Study & Design

Study Type
Interventional study
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Hemodynamics of the anterior ciliary artery;Hemodynamics of the central retinal artery;Eye symptom score for individual and total scores;
Secondary Outcome Measures
NameTimeMethod
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