About this trial
The goal of this observational study is to learn about the 6-month effects of Levator Resection combined with Fascial Sheath Suspension surgery in patients who undergo this procedure to treat congenital ptosis. The main questions it aims to answer are:
Does this combined surgery improve best-corrected visual acuity, stereopsis, and other visual function indicators in patients with congenital ptosis within 6 months after the operation?
Does this surgery lead to an improvement in patient-reported quality of life during the same period?
Patients already scheduled to undergo this combined surgery as part of their regular medical care for congenital ptosis will complete a series of standardized ophthalmological examinations and a quality of life questionnaire before surgery and at 1, 3, and 6 months post-operation.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Unilateral or bilateral congenital ptosis, male or female;
Age: 3-60 years old
Informed consent, and voluntary signing of the informed consent form, in compliance with ethical norms
Disqualifiers
None
Trial population
The plan is to continuously enroll newly diagnosed or unoperated patients from the Ophthalmic Plastic Surgery Clinic of the Sun Yat-sen University Eye Center, and simultaneously invite accompanying individuals as a control group
Trial design
Cohort
Prospective
Treatments tested in this trial
Not listed
Trial groups
Trial outcomes
Primary outcomes
stereoacuity
Sponsors and contacts
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