Clinical Trials Directory

Trials / Recruiting

RecruitingNCT07387536

The Effectiveness of Topical Silicone Application Combined With Photoprotection in the Development of Scarring Following Blepharoplasty

Status
Recruiting
Phase
Phase 4
Study type
Interventional
Enrollment
30 (estimated)
Sponsor
Instituto de Oftalmología Fundación Conde de Valenciana · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Assess the efficacy of utilizing topical silicone with photoprotection (Improscar Stick® 50) on the quality of healing following upper blepharoplasty, employing the Vancouver and POSAS scales (both patient and observer) over a minimum follow-up period of three months.

Detailed description

This study is a clinical, experimental, prospective, and comparative before-and-after investigation involving participants undergoing upper blepharoplasty. Individuals aged between 18 and 70 years will be included in the study. Clinical assessments will be conducted at four distinct time points: one week postoperatively (coinciding with suture removal and the initiation of treatment), one week following the commencement of treatment, at one month, and three months post-treatment. The Vancouver and POSAS scales, both subjective and objective, will be employed for evaluation. For inferential analysis, ANOVA for repeated measures will be utilized, employing IBM SPSS Statistics v31.0 software. Any adverse effects will be documented.

Conditions

Interventions

TypeNameDescription
DRUGSilicone-based topical formulation with sunscreen (SPF 50) applicationSilicone-based topical formulation with sunscreen (SPF 50), will be administered to the eyelid incisions of research participants who have undergone blepharoplasty.

Timeline

Start date
2025-10-01
Primary completion
2026-03-31
Completion
2026-05-31
First posted
2026-02-04
Last updated
2026-02-04

Locations

1 site across 1 country: Mexico

Source: ClinicalTrials.gov record NCT07387536. Inclusion in this directory is not an endorsement.