Intense Pulsed Light in Meibomian Gland Dysfunctions

NCT ID: NCT04147962

Last Updated: 2022-05-13

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

45 participants

Study Classification

OBSERVATIONAL

Study Start Date

2019-10-25

Study Completion Date

2020-06-01

Brief Summary

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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.

Detailed Description

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Conditions

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Dry Eye Syndromes Meibomian Gland Dysfunction

Study Design

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Observational Model Type

COHORT

Study Time Perspective

RETROSPECTIVE

Study Groups

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Patients with dry eye disease with meibomian gland dysfunction

Collected data from patient records for consultations Day 0, Day 15 and Day 45 (3 treatment sessions) and Months 3, Months 6 (follow-up consultations).

\- parameters used for each treatment session: duration of treatment session and intensity of intense pulsed light

intense pulsed light (usual practice)

Intervention Type DEVICE

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

Interventions

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intense pulsed light (usual practice)

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

Intervention Type DEVICE

Eligibility Criteria

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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
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Quantel Medical

INDUSTRY

Sponsor Role collaborator

Centre Hospitalier Universitaire de Saint Etienne

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Marie Caroline TRONE, MD

Role: PRINCIPAL_INVESTIGATOR

CHU de Saint Etienne

Locations

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CHU de Saint Etienne

Saint-Etienne, , France

Site Status

Countries

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France

References

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Trone MC, Garcin T, Ollier E, Thuret G, Gain P. A retrospective study of the efficacy of intense pulsed light delivered by the Lacrystim(R) for meibomian gland dysfunction therapy. BMC Ophthalmol. 2022 Aug 6;22(1):335. doi: 10.1186/s12886-022-02531-7.

Reference Type DERIVED
PMID: 35933379 (View on PubMed)

Other Identifiers

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IRBN672019/CHUSTE

Identifier Type: -

Identifier Source: org_study_id

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