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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05449015
Other study ID # 2022SQ006
Secondary ID
Status Recruiting
Phase Phase 4
First received
Last updated
Start date December 22, 2020
Est. completion date June 2023

Study information

Verified date December 2022
Source Shanghai Eye Disease Prevention and Treatment Center
Contact Yan Xu, M.D.
Phone +86 18621080996
Email drxuyan_2004@163.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Atropine has a ciliary muscle-paralysing effect and causes hyperopic drift. Besides, atropine has been proven to slow the progression of myopia. Many studies have suggested that atropine can increase the thickness of the choroid. However, few studies have discussed changes in the ciliary muscle after treatment with atropine or other cycloplegic agents. This study aimed to assess the difference in ciliary muscle morphology before and after two different cycloplegic agents and to analyze the correlation between the changes of ciliary muscle biological parameters and the changes of eye axis, spherical equivalent, lens diopter, choroidal thickness, etc. One hundred and forty-four children would be randomly assigned 1:1 to the 1% atropine group and the tropicamide group. This study might provide clinical evidence for the role of regulatory factors in the occurrence and development of myopia.


Description:

The ciliary muscle exhibited an inward-forward contraction during accommodation, resulting in a significant thickening of the anterior area of the ciliary muscle. In addition to ultrasound biomicroscope (UBM), anterior segment optical coherence tomography (AS-OCT) is also commonly used to study morphological changes in the ciliary muscle. Studies using AS-OCT revealed that the posterior area of the ciliary muscle thinned during accommodation. The morphology of the ciliary muscles differs in individuals with refractive errors. Many researchers found that the ciliary muscle became thicker with an increase of axial length (AL) Some studies suggested that myopia primarily affected the posterior area of the ciliary muscle. Atropine has a ciliary muscle-paralysing effect and causes hyperopic drift. Besides, atropine has been proven to slow the progression of myopia. Many studies have suggested that atropine can increase the thickness of the choroid. However, few studies have discussed changes in the ciliary muscle after treatment with atropine or other cycloplegic agents. This study aimed to assess the difference in ciliary muscle morphology before and after two different cycloplegic agents and to analyze the correlation between the changes of ciliary muscle biological parameters and the changes of eye axis, spherical equivalent, lens diopter, choroidal thickness, etc. One hundred and forty-four children would be randomly assigned 1:1 to the 1% atropine group and the tropicamide group. This study might provide clinical evidence for the role of regulatory factors in the occurrence and development of myopia.


Recruitment information / eligibility

Status Recruiting
Enrollment 144
Est. completion date June 2023
Est. primary completion date March 2023
Accepts healthy volunteers No
Gender All
Age group 3 Years to 12 Years
Eligibility Inclusion Criteria: - ?Age 3 to 12 years old; - Astigmatism <2.00D, binocular anisometropia <3.00D, and the best corrected distance visual acuity is at least 0.8, near vision at least 0.8; - A clear anterior segment image can be obtained through anterior segment OCT; - Have normal thinking and language communication skills, and can actively cooperate with the inspection process; ? No contraindications to atropine treatment such as acute eye inflammation, dry eye, keratoconus, diabetes, etc.; ?Written informed consent of the guardian and the child himself Exclusion Criteria: - ? Combined with neurological diseases and have allergies or contraindications to cycloplegic drugs or other drugs; - Intraocular pressure =21mmHg; history of photosensitivity, glaucoma, blue eye syndrome, ocular hypertension, and retinal macular lesions or damage; - Patients with chronic eye diseases such as ocular trauma and allergic conjunctivitis; - Those who wear contact lenses and those who use myopia control-related drugs within 1 month; ? Patients with previous varus trichiasis, severe horn, conjunctiva infection and other eye diseases; - Insufficient image quality, such as inconsistent field of view, poor image exposure, inaccurate image focus, stains, shadows or crescent shadows, etc.; - There are systemic diseases; ? Epilepsy, mental disorders unable to communicate normally; ? Other circumstances judged by the investigator to be unsuitable to participate in the research

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
1% atropine
Daily application can be used for mydriasis and refraction examination Weekly long-term application can be used to control myopia

Locations

Country Name City State
China Shanghai Eye Diseases Prevention & Treatment Center Shanghai Shanghai

Sponsors (1)

Lead Sponsor Collaborator
Shanghai Eye Disease Prevention and Treatment Center

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Other choroidal thickness choroidal thickness, microns(um), measured by SSOCT before intervention
Other choroidal thickness choroidal thickness, microns(um), measured by SSOCT immediately after the last intervention
Other lens thickness lens thickness(LT), millimeter(mm), measured by IOL master before intervention
Other lens thickness lens thickness(LT), millimeter(mm), measured by IOL master immediately after the last intervention
Other lens power lens power(LP), diopter(D), calculated by Bennett formula before intervention
Other lens power lens power(LP), diopter(D), calculated by Bennett formula immediately after the last intervention
Other corneal parameters central corneal thickness(CTC), micron(um), measured by IOL master before intervention
Other corneal parameters central corneal thickness(CTC), micron(um), measured by IOL master immediately after the last intervention
Other retinal thickness retina thickness, microns(um), measured by SSOCT before intervention
Other retinal thickness retina thickness, microns(um), measured by SSOCT immediately after the last intervention
Primary ciliary thickness parameters ciliary thickness parameters, microns(um), photographed by ASOCT and measured by semiautomatic software before intervention
Primary ciliary thickness parameters ciliary thickness parameters, microns(um), photographed by ASOCT and measured by semiautomatic software immediately after the last intervention
Primary the distance between ciliary muscle apex and scleral spur ciliary muscle thickness, microns(um), photographed by ASOCT and measured by semiautomatic software before intervention
Primary the distance between ciliary muscle apex and scleral spur ciliary muscle thickness, microns(um), photographed by ASOCT and measured by semiautomatic software immediately after the last intervention
Secondary spherical equivalent spherical equivalent(SE),Diopter(D), measured by subjective optometry before intervention
Secondary spherical equivalent spherical equivalent(SE),Diopter(D), measured by subjective optometry immediately after the last intervention
Secondary axial length axial length(AL), millimeter(mm), measured by IOL master before intervention
Secondary axial length axial length(AL), millimeter(mm), measured by IOL master immediately after the last intervention
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