- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07481695
Retrospective Follow-up Study on Lower Eyelid Melanin and Wrinkles After Blepharoplasty for Lower Eyelid Bags
This observational study aims to investigate the long-term outcomes of transconjunctival lower eyelid blepharoplasty, with a specific focus on changes in lower eyelid hyperpigmentation or hypopigmentation and morphological alterations of wrinkles at short-term and long-term postoperative time points. It further seeks to clarify the overall impact of this surgical approach on lower eyelid skin appearance.
The study addresses the following research questions:
Does transconjunctival lower eyelid blepharoplasty improve lower eyelid pigmentation? If so, to what extent is the improvement achieved? Does transconjunctival lower eyelid blepharoplasty exacerbate lower eyelid wrinkles? What adjunctive or combined surgical techniques may mitigate this effect? All study participants had previously undergone transconjunctival lower eyelid blepharoplasty for the purpose of periorbital rejuvenation.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Tianjin, China
- Tianjin Eye Hospital
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
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Transconjunctival lower blepharoplasty
conventional transconjunctival lower blepharoplasty, this conventional approach combined of transconjunctival intraorbital fat excision and fat transplantation.
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Transconjunctival lower blepharoplasty is a minimally invasive surgical technique for lower eyelid rejuvenation.
It accesses orbital fat through an internal conjunctival incision, avoiding external skin scars.
It reduces fat prolapse, improves tear trough deformity, and preserves lower eyelid support, ideal for patients with prominent fat bags and minimal skin laxity.
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Transconjunctival lower blepharoplasty combined with POD lifting
conventional transconjunctival lower blepharoplasty combined POD lifting in order to alleviate postoperative skin laxity.
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Transconjunctival lower blepharoplasty is a minimally invasive surgical technique for lower eyelid rejuvenation.
It accesses orbital fat through an internal conjunctival incision, avoiding external skin scars.
It reduces fat prolapse, improves tear trough deformity, and preserves lower eyelid support, ideal for patients with prominent fat bags and minimal skin laxity.
POD lifting is a minimally invasive facial lifting procedure using absorbable polydioxanone sutures.
It elevates sagging soft tissues by creating mechanical support and stimulating collagen production.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Barton's grading scale
Time Frame: Before the operation, and six months after the operation
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The Barton Grading Scale is a validated clinical tool standardized for assessing the severity of lower eyelid contour deformities, particularly tear troughs and lower eyelid bags.
It operates on a numeric or alphanumeric scale, typically ranging from 0 to 4 or Grade I to III, to quantify the depth of the tear trough and the degree of orbital fat prolapse.
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Before the operation, and six months after the operation
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Global Aesthetic Improvement Scale
Time Frame: Before the operation, and six months after the operation
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Global Aesthetic Improvement Scale (GAIS) is a validated 5-point subjective scale used to evaluate overall facial aesthetic improvement from baseline, widely applied in clinical trials and skincare research.
Raters (clinicians or participants) score from 1 (markedly improved) to 5 (much worse), often with a neutral midpoint.
It complements objective measures by assessing holistic changes in wrinkles, skin laxity, tone, and texture.
Standardized training ensures inter-rater reliability.
GAIS is integral to quantifying treatment effects in periorbital rejuvenation and anti-aging studies, providing actionable global outcomes.
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Before the operation, and six months after the operation
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Periorbital hyperpigmentation assessment
Time Frame: Before the operation and six months after the operation
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Periorbital hyperpigmentation assessment includes both qualitative and quantitative evaluation.
Qualitative assessment uses a 5-point scale: 0 = matched facial skin color; 1 = mild periorbital pigmentation; 2 = obvious pigmentation; 3 = severe dark color involving upper and lower eyelids; 4 = severe pigmentation extending beyond the infraorbital fold.
Quantitative assessment compares pre- and postoperative grayscale values derived from standardized clinical photographs.
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Before the operation and six months after the operation
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Wrinkles in the lower eyelid
Time Frame: Before the operation and six months after the operation.
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Wrinkles in the lower eyelid are evaluated using a quantitative method.
The number and length of lower eyelid wrinkles are measured and calculated.
Preoperative and postoperative changes are objectively compared to assess the surgical effect on wrinkle improvement.
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Before the operation and six months after the operation.
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Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 2026(084)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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