To develop a feedback-enabled magnetic device for management of blepharoptosis and evaluate its efficacy and safety, including the gain of palpebral fissure height, visual field obstruction, blurred vision, foreign body sensation over the cornea, burning or hot sensation over facial skin, and erythema or pruritus over the eyelid, by performing a human trial on patients with blepharoptosis.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Patients with ptosis; they are capable of understanding and complying with protocol requirements
* Aged 18 years old or older
Exclusion Criteria:
* Upper eyelid scar, contracture, or fibrosis due to previous surgical intervention(s)
* Patients with psychiatric (or mental) di…
Inclusion Criteria:
* Patients with ptosis; they are capable of understanding and complying with protocol requirements
* Aged 18 years old or older
Exclusion Criteria:
* Upper eyelid scar, contracture, or fibrosis due to previous surgical intervention(s)
* Patients with psychiatric (or mental) disorders; they are unable to cooperate or follow the study procedure
* Children younger than 18 years of age
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