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Sterile Plant-Based Gauze for Eyelid Hygiene in Anterior Blepharitis

A Prospective Randomized Controlled Trial of a Sterile Gauze Containing Natural Plant Extracts (Leniben®) for Eyelid Hygiene in Patients With Bilateral Anterior Blepharitis

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07759180
Acronym
BLEPH-GAUZE
Enrollment
38
Registered
2026-08-12
Start date
2023-02-02
Completion date
2025-12-12
Last updated
2026-08-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Blepharitis

Keywords

Anterior blepharitis, eyelid hygiene, eyelid microbiota, eyelid wipes

Brief summary

The goal of this clinical trial is to learn whether a sterile gauze containing natural plant extracts can lower the number of bacteria on the eyelid margin in people with bilateral anterior blepharitis. The study will also evaluate whether the product is safe and well tolerated after a single application. The main questions it aims to answer are: * Does the sterile gauze containing natural plant extracts reduce the bacterial load on the eyelid margin more than a standard sterile gauze? * Does the treatment improve eyelid comfort without causing unwanted side effects? Researchers will compare the study gauze with a sterile gauze without active ingredients. Each participant will receive both treatments: the right eye will be treated with the study gauze, while the left eye will be treated with the control gauze. This allows each participant to serve as their own control. Participants will: * Attend one study visit. * Undergo an eye examination to confirm the diagnosis of bilateral anterior blepharitis. * Have samples collected from the upper and lower eyelid margins of both eyes before treatment. * Receive eyelid cleansing with the assigned gauze for each eye. * Have eyelid samples collected again 20 minutes after treatment. * Complete a short questionnaire about treatment comfort and tolerability. The study will compare the change in bacterial growth between the two eyes to determine whether the natural plant-based gauze provides additional microbiological benefits beyond mechanical eyelid cleansing alone. Safety and participant comfort will also be assessed.

Detailed description

Anterior blepharitis is a chronic inflammatory disorder of the eyelid margin characterized by erythema, scaling, crusting, and ocular discomfort. The condition is frequently associated with increased bacterial colonization of the eyelid margin, particularly by Staphylococcus aureus and coagulase-negative staphylococci, which contribute to chronic inflammation through the production of lipases, proteases, and other virulence factors. Bacterial biofilm formation further promotes microbial persistence and recurrent disease, making eyelid hygiene a fundamental component of long-term management. Although mechanical cleansing of the eyelid margin is widely recommended, limited clinical evidence is available regarding the immediate microbiological efficacy of sterile eyelid cleansing devices containing natural plant-derived compounds. Leniben® Gauze is a sterile single-use cotton gauze impregnated with sodium hyaluronate, Echinacea angustifolia extract, Ananas sativus extract (bromelain), ammonium glycyrrhizate, and tocopherol. The device is intended to combine the mechanical removal of eyelid debris and microbial biofilm with the moisturizing and soothing properties of its active ingredients. This prospective, randomized, paired-eye controlled clinical trial is designed to evaluate the microbiological efficacy of Leniben® Gauze in adults with bilateral anterior blepharitis. Each participant serves as his or her own control: the right eye receives treatment with Leniben® Gauze, while the contralateral eye is treated with an identical sterile cotton gauze moistened with sterile saline solution. This paired-eye design minimizes inter-individual variability in eyelid microbiota and allows direct comparison between the active formulation and mechanical cleansing alone. Microbiological samples are collected from the upper and lower eyelid margins of both eyes immediately before treatment and 20 minutes after the cleansing procedure. Samples are cultured using standard microbiological techniques, and bacterial growth is quantified as colony-forming units (CFU). Changes in bacterial load and bacterial eradication rates are compared between treatments. Participant-reported tolerability and any treatment-related adverse events are also assessed. The results of this study will provide evidence on the ability of a plant-based sterile eyelid cleansing device to reduce periocular bacterial colonization and may support its use as a non-antibiotic adjunctive strategy for eyelid hygiene in anterior blepharitis and for reducing bacterial burden before ophthalmic procedures.

Interventions

DEVICEPlant-Based Sterile Eyelid Gauze

Participants received eyelid hygiene using Leniben® Gauze, a sterile single-use cotton gauze impregnated with a solution containing sodium hyaluronate, Echinacea angustifolia extract, Ananas sativus extract (bromelain), ammonium glycyrrhizate, and tocopherol. One eye of each participant was randomly assigned to the intervention. The upper and lower eyelid margins were cleansed using five standardized strokes, and microbiological samples were collected before treatment and 20 minutes after application to evaluate changes in bacterial colonization.

DEVICESterile Cotton Gauze Moistened with Saline Solution

Participants received eyelid hygiene using an identical sterile single-use cotton gauze moistened with sterile saline solution, without active ingredients. The contralateral eye of each participant was randomly assigned to the control treatment. The upper and lower eyelid margins were cleansed using the same standardized procedure as the experimental arm (five standardized strokes). Microbiological samples were collected before treatment and 20 minutes after application to evaluate changes in bacterial colonization attributable to mechanical cleansing alone

Sponsors

Azienda Ospedaliera OO.RR. S. Giovanni di Dio e Ruggi D'Aragona
Lead SponsorOTHER
Federico II University
CollaboratorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Masking description

This is a prospective, randomized, paired-eye controlled trial in which each participant serves as his or her own control. For each participant, one eye was randomly assigned to treatment with Leniben® Gauze containing natural plant extracts, while the contralateral eye was randomly assigned to treatment with an identical sterile cotton gauze moistened with sterile saline. Microbiological outcomes were compared within the same participant, thereby minimizing inter-individual variability in eyelid bacterial colonization and improving the precision of treatment effect estimates.

Intervention model description

This is a prospective, randomized, paired-eye controlled trial in which each participant serves as his or her own control. For each participant, one eye was randomly assigned to treatment with Leniben® Gauze containing natural plant extracts, while the contralateral eye was randomly assigned to treatment with an identical sterile cotton gauze moistened with sterile saline. Microbiological outcomes were compared within the same participant, thereby minimizing inter-individual variability in eyelid bacterial colonization and improving the precision of treatment effect estimates.

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Adults aged 18 years or older. * Clinical diagnosis of bilateral anterior blepharitis confirmed by slit-lamp examination. * Presence in both eyes of eyelid-margin inflammation associated with at least two of the following clinical signs: eyelid-margin hyperemia; eyelash crusting or collarettes; scaling or debris at the base of the eyelashes; lash abnormalities; mucocutaneous inflammation. * Presence of at least one associated symptom, including burning, itching, foreign-body sensation, tearing, or ocular irritation. * Ability and willingness to provide written informed consent.

Exclusion criteria

* Active ocular infection other than anterior blepharitis. * Predominantly posterior blepharitis requiring specific treatment. * Clinically evident Demodex infestation. * Ocular surgery within the previous 3 months. * Contact lens wear. * Use of topical or systemic antibiotics, antiseptics, or corticosteroids within the previous 4 weeks. * Ocular trauma. * Autoimmune disease or immunodeficiency. * Pregnancy or breastfeeding. * Known hypersensitivity to any component of the study products.

Design outcomes

Primary

MeasureTime frameDescription
Difference in Post-Treatment Eyelid Bacterial Load Adjusted for BaselineBaseline and 20 minutes after a single treatmentBaseline-adjusted difference in total eyelid-margin bacterial load 20 minutes after cleansing between eyes treated with a sterile gauze containing natural plant extracts and contralateral eyes treated with sterile saline-moistened gauze. Total bacterial load is defined as the sum of colony-forming units per milliliter (CFU/mL) of all bacterial species isolated from each eye and analyzed after log₁₀(CFU/mL + 1) transformation.

Secondary

MeasureTime frameDescription
Culture-Negative Conversion20 minutes after a single treatmentProportion of eyes with a positive baseline culture that convert to no detectable bacterial growth 20 minutes after treatment. Culture-negative conversion is defined as the transition from a positive baseline culture to no detectable bacterial growth after cleansing.
Percentage Reduction in Eyelid Bacterial LoadBaseline and 20 minutes after a single treatmentPercentage reduction in total bacterial load from baseline to 20 minutes after treatment, calculated only for eyes with a positive baseline culture. Total bacterial load is expressed as colony-forming units per milliliter (CFU/mL).
Changes in Eyelid Microbiological ProfileBaseline and 20 minutes after a single treatmentQualitative and quantitative changes in bacterial species isolated from eyelid-margin cultures, including persistence, clearance, or changes in polymicrobial colonization after treatment. Species-specific analyses are exploratory.
Treatment Comfort and TolerabilityImmediately after treatmentParticipant-reported ocular comfort, treatment tolerability, and overall acceptability assessed immediately after treatment using 5-point Likert scales, where 1 = very uncomfortable, 2 = uncomfortable, 3 = neutral, 4 = comfortable, and 5 = very comfortable. Higher scores indicate greater treatment comfort and tolerability.
Treatment-Related Adverse EventsFrom treatment administration until completion of the study visit (20 minutes)Incidence of ocular or periocular adverse events, including burning, stinging, itching, tearing, blurred vision, conjunctival hyperemia, eyelid erythema or edema, and corneal epithelial abnormalities occurring after treatment.

Countries

Italy

Contacts

PRINCIPAL_INVESTIGATORMario Troisi, MD

Azienda Ospedaliera Universitaria OO.RR. S. Giovanni di Dio e Ruggi D'Aragona, Salerno, Italy

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 13, 2026