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NCT06363422 Clinical Trial

The Value of Epicanthoplasty on the Modification of Upper-eyelid Appearance

Patient Satisfaction Clinical Trial

Official title:
The Value of Epicanthoplasty on the Modification of Upper-eyelid Appearance: a Retrospective Study

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT06363422
Other study ID # JY2024-012
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 1, 2024
Est. completion date April 1, 2024

Study information
Verified date April 2024
Source Shanghai Ninth People's Hospital Affiliated to Shanghai Jiao Tong University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

In East Asian populations, the combination of an epicanthic fold and mono-eyelid is one of their anatomical characteristics. Misalignment of the orbicularis oculi muscle and fibrous connections leads to longitudinal tension, forming the epicanthic fold. The epicanthic fold may diminish the aesthetic effects of eyelid cosmetic surgery, shorten the horizontal length, and affect the postoperative shape of double eyelids. As upper eyelid cosmetic surgery is one of the most common cosmetic procedures in Asia, there is increasing attention on the modification of the epicanthic fold and its impact on the formation of double eyelids.

Recruitment information / eligibility
Status Completed
Enrollment 14
Est. completion date April 1, 2024
Est. primary completion date March 15, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - 1: Patients who have previously undergone unsatisfactory blepharoplasty, combined with epicanthic fold issues; 2: Underwent epicanthoplasty in this center 3: over 18-year-old and less than 60-year-old 4: Clinical data was comprehensive. Exclusion Criteria: - 1: The patient has concurrent untreated lacrimal defects, excessive eyelid skin, and other complications such as entropion and ectropion.

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• Epicanthoplasty
Patients with unsatisfied blepharoplasty underwent epicanthoplasty in our center

Locations
Country Name City State
China Shanghai ninth people's hospital Shanghai

Sponsors (1)
Lead Sponsor Collaborator
Shanghai Ninth People's Hospital Affiliated to Shanghai Jiao Tong University

Country where clinical trial is conducted

China, 

Outcome
Type Measure Description Time frame Safety issue
Primary inter-epicanthal distance (IED) The inter epicanthal distance was measured by the distance from left to right epicanthus. preoperatively and through study completion, an average of 1 year
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