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Intense Pulsed Light in Meibomian Gland Dysfunctions

Intense Pulsed Light in Meibomian Gland Dysfunctions: Retrospective Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04147962
Acronym
LACRYSTIM
Enrollment
45
Registered
2019-11-01
Start date
2019-10-25
Completion date
2020-06-01
Last updated
2022-05-13

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

Conditions

Dry Eye Syndromes, Meibomian Gland Dysfunction

Keywords

intense pulsed light

Brief summary

Dry eye disease (DED) is an extremely common disease whose meibomian gland dysfunction is the main etiology. Polychromatic intense pulsed light (IPL) is a promising new therapeutic alternative but few clinical data have been published. A new IPL device has recently been marketed: LACRYSTIM (QUANTEL, France). The investigators have been using it in our clinical practice since June 2019. The investigators present a retrospective study on our first clinical results.

Interventions

DEVICEintense pulsed light (usual practice)

collection data : parameters used for each treatment session: duration of treatment session and intensity of intense pulsed light

Sponsors

Quantel Medical
CollaboratorINDUSTRY
Centre Hospitalier Universitaire de Saint Etienne
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

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

Inclusion criteria

* Patients with Dry eye disease with meibomian gland dysfunction, preferentially mild to moderate, and having benefited from intense pulsed light treatment. * patient affiliated with a social security organization

Exclusion criteria

* patient with incomplete follow-up

Design outcomes

Primary

MeasureTime frameDescription
Lacrydiag in current clinical practice6 monthsThe LacryDiag ocular surface analyzer is used for the diagnosis of dry eyes.

Secondary

MeasureTime frameDescription
Ocular Surface Disease Index questionnaire6 monthsmeasured in current clinical practice. This 12-item questionnaire assesses dry eye symptoms and the effects it has on vision-related function in the past week of the patient's life. The questionnaire has 3 subscales: ocular symptoms, vision-related function, and environmental triggers.
Slit lamp Photography x16 and x256 monthsin current clinical practice
collection of adverse events6 months-data concerning the safety: presence or absence of adverse events during treatment or afterwards (burns, tingling, redness of skin ...)
Break-up time Test6 monthsmeasured in current clinical practice. The measurement of the tear film rupture time determines the stability of the tear film, i.e. the degree of humidification of the eyes.
Schirmer Test6 monthsmeasured in current clinical practice. Determination of the quantity of tears produced.
Oxford Score6 monthsmeasured in current clinical practice. The Oxford score is used to assess epithelial damage to the cornea and conjunctiva.

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 11, 2026