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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05962528
Other study ID # KY2023024
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date April 1, 2023
Est. completion date December 1, 2024

Study information

Verified date July 2023
Source Tianjin Eye Hospital
Contact Tiejing Sun, MD
Phone +8627306525
Email suntiejing0109@163.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To evaluate whether there is a difference in subjective and objective fit of soft lenses with different sagittal height


Recruitment information / eligibility

Status Recruiting
Enrollment 60
Est. completion date December 1, 2024
Est. primary completion date July 1, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 50 Years
Eligibility Inclusion Criteria: - Age more than 18 years - No active eye disease - 5 soft lenses for the experiment can be successfully worn and all examinations can be completed as required Exclusion Criteria: - Active eye disease - BCVA less than 20/25 - Those who are too small or tight eyelids are not suitable for wearing soft lenses

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Soft lens
Patients were randomly fitted with five different designs of soft lenses

Locations

Country Name City State
China Tianjin Eye Hospital Tianjin

Sponsors (1)

Lead Sponsor Collaborator
Tianjin Eye Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Subjective questionnaire The subjective questionnaire is a visual quality questionnaire developed by combining previous research and clinical symptoms, including whether there is foreign body sensation, pain, dry eyes, etc.The score ranges from 0 to 4, with the higher the score, the more obvious the symptoms 1 day (Once time after wearing the soft lens)
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