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Probiotics for Treatment of Chalazion in Adults

Effects of Probiotic Oral Supplementation on the Treatment of Chalazion in Adults: a Pilot Study on 20 Patients

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04342507
Enrollment
20
Registered
2020-04-13
Start date
2019-02-01
Completion date
2020-02-29
Last updated
2020-04-14

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

Conditions

Chalazion

Keywords

microbiome/microbiota, probiotics, adults

Brief summary

There is growing evidence encouraging probiotics use in several diseases. The aim of the investigator's study is to define the possible beneficial impact of probiotics on adults suffering from chalazia.

Detailed description

Prospective comparative pilot study on 20 adults suffering from chalazion randomly divided into two groups. The first group, received conservative treatment with lid hygiene, warm compression, and dexamethasone/tobramycin ointment for at least 20 days. The second group, in addition to the conservative treatment, received a mixture of probiotic microorganisms once a day up to 3 months. Chalazia were classified according to their size into three groups: small (≤2 mm), medium (2-4 mm), or large (\>4 mm). When conservative treatment (with and without probiotics supplementation) failed to resolve the lesion, invasive methods were used, (intralesion steroid injection in medium size chalazion and surgical incision and curettage for the largest ones).

Interventions

OTHERconservative treatment

lid hygiene, warm compression, and dexamethasone/tobramycin ointment for at least 20 days.

DIETARY_SUPPLEMENTprobiotics

use specific probiotics in addiction to conservative treatment to modify the intestinal microbiome to ameliorate the clinical course of adults chalazia by re-establishing intestinal and immune homeostasis

Sponsors

University of Molise
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
TRIPLE (Caregiver, Investigator, Outcomes Assessor)

Intervention model description

Prospective comparative pilot study with two groups randomly divided

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* history of rapid onset of painful inflamed mass that had reached a stationary size for more than 2 months * clinical appearance and location of the lesion

Exclusion criteria

* eyelid infection * chalazion duration \< 1 month * nonpalpable chalazion * suspicion of malignancy * comorbidities (constitutional atopy and seborrheic dermatitis, hormonal dysfunction, presence of irritable bowel disease, infectious mainly related to Staphylococcus aureus and Propionibacterium acnes, demodex mite infestation, vitamin A deficiency, arterial hypertension, diabetes and pregnancy) * personal habits (smoking, eating disorders, etc.)

Design outcomes

Primary

MeasureTime frameDescription
healing time3 monthshealing time changes with a complete resolution of chalazion

Secondary

MeasureTime frameDescription
recurrencessix monthsevaluation of recurrences in both arms

Countries

Italy

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026