Beyoglu Eye Training and Research Hospital
Istanbul, 34421, Turkey (Türkiye)
NCT Number: NCT07701265
This study evaluated whether applying a compression dressing to one eyelid after upper eyelid blepharoplasty (eyelid lift surgery) reduces swelling, bruising, and discomfort compared to the untreated eyelid. In this randomized trial, each participant underwent bilateral upper eyelid blepharoplasty; after surgery, one eyelid was randomly assigned to receive a compression dressing for 24 hours, while the other eyelid received no dressing and served as the internal control. Outcomes including eyelid swelling, bruising, pain, aesthetic appearance, and corneal health were assessed by masked observers on postoperative days 1, 7, 30, and 90. The goal of this study was to determine whether routine use of compression dressing provides a measurable clinical benefit after this common cosmetic and functional eyelid surgery.
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Notify Me18 year and older
All sexes
Interventional
Not applicable
Istanbul, 34421, Turkey (Türkiye)
This was a prospective, randomized, controlled, observer-masked, within-subject (split-eye) trial conducted at a single academic center between June and November 2025. Adult patients with bilateral dermatochalasis scheduled for upper eyelid blepharoplasty were enrolled. Following bilateral surgery performed by a single surgeon, one eyelid of each patient was randomly assigned by coin toss to receive a compression dressing (folded sterile gauze secured with elastic tape, left in place for 24 hours), while the contralateral eyelid received no dressing and served as the internal control. All patients received standardized postoperative care, including bilateral cold compresses and topical medications.
Two masked investigators independently assessed postoperative edema (5-point ordinal scale), ecchymosis (ImageJ-based area quantification), and aesthetic outcome (Global Aesthetic Improvement Scale) from standardized clinical photographs obtained on postoperative days 1, 7, 30, and 90; disagreements were resolved by a third masked investigator. Postoperative pain (visual analog scale) and patient comfort preference were recorded on day 1. Best corrected visual acuity and corneal fluorescein staining (Oxford grading scale) were assessed at each follow-up visit to evaluate ocular surface safety. Between-group comparisons were performed using the Wilcoxon signed-rank test, with Holm-Bonferroni correction applied across outcomes at each visit to account for multiple comparisons.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
A compression dressing consisting of folded sterile gauze pads followed by a dry gauze layer, secured with elastic tape (Clivex®, Climed Healthcare, Türkiye), applied to one upper eyelid immediately after bilateral upper eyelid blepharoplasty and left in place for 24 hours. The contralateral eyelid remained uncovered and undressed, serving as the internal control.
The contralateral upper eyelid received standard postoperative care without a compression dressing, remaining uncovered. All other postoperative treatments (topical antibiotic ointment, cooling protocol, medications) were identical to the compression dressing side.
Time frame: Postoperative day 1, postoperative day 7, postoperative day 30, postoperative day 90
Standardized clinical photographs assessed by masked observers using a 5-point ordinal edema grading scale.
Time frame: Postoperative day 1, postoperative day 7, postoperative day 30, postoperative day 90
Standardized clinical photographs analysed using ImageJ software and graded by masked observers.
Time frame: Postoperative day 1
Visual analogue scale (0-10)
Time frame: Postoperative day 1
Patient questionnaire comparing comfort between the compression dressing and control eyelids.
Time frame: Postoperative days 1, 7, 30 and 90
Fluorescein staining graded according to the Oxford grading scale.
Time frame: Postoperative days 1, 7, 30 and 90
Global Aesthetic Improvement Scale assessed by masked observers using standardized clinical photographs.
Time frame: Baseline, postoperative days 1, 7, 30 and 90
Best corrected visual acuity measured in logarithm of the minimum angle of resolution units.
Fatma Poslu Karademir
Other Gov
The Effect of Compression Dressing on Postoperative Outcomes After Upper Eyelid Blepharoplasty: A Randomized, Controlled, Observer-Blinded Evaluation Study
Acronym: COMPRESS-BLEPH
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