Comparison Between Continuous and Pulsed Oral Doxycycline Treatment Protocols for Refractory Meibomian Gland Dysfunction

NCT ID: NCT06520007

Last Updated: 2024-07-25

Basic Information

• Recruitment Status: COMPLETED
• Total Enrollment: 65 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2023-03-01
• Study Completion Date: 2024-05-01

Brief Summary

The goal of this observational study (spontaneous, non-randomised, prospective cohort, phase IV) is to compare the efficacy and safety of two different oral doxycycline treatment protocols (LCP - Low dose continuous protocol & FPP - Full dose pulsed protocol) for meibomian gland dysfunction (MGD) in patients with refractory MGD (OSDI > 13 after at least 2 months treatment with warm compresses and lacrimal substitutes - first-line therapy). Systemic doxycycline doesn't have a standardized treatment protocol and this is why those patients are treated as in normal clinical practice. The main questions it aims to answer are:

Which treatment protocol has a greater impact on patient symptoms during the follow-up (OSDI score reduction)? Which treatment protocol has a greater impact on patient signs during the follow-up (TBUT and corneal staining variations)? Which treatment protocol is safer (in terms of adverse events rate)?

Participants will be visited every 3 months (V0-V1-V2-V3) with signs and symptoms assessment (TBUT, corneal staining, OSDI score) after being treated for 3 months with the assigned doxycycline treatment protocol (LCP or FPP).

Detailed Description

This spontaneous, prospective, non-randomized, parallel-group, phase IV study was conducted in compliance with the tenets of the Declaration of Helsinki.

All study participants were fully consented, and written informed consent was obtained.

This study included patients with refractory MGD. Refractory MGD is defined as symptomatic MGC (OSDI > 13 points) despite 2 months of first-line treatment with lacrimal substitutes 3 times per day and meibomian gland expression with warm compresses twice per day.

The study will consist of 3 visits: Baseline (day 0), Visit 2 (day 90 ± 5 - 3rd month), Visit 3 (day 180 ± 5 - 6 month). At each visit, patients will receive an OSDI questionnaire, NIBUT, type I Schirmer test and AS assessment, including TBUT, corneal staining (Oxford scale) At baseline, eligible patients will be enrolled and treated with the assigned protocol. The investigators will assign the protocol (non-randomized) in a 1:1 ratio.

At Visit 2, NIBUT, TBUT, Oxford scale and OSDI improvement will be evaluated compared with Visit 1. Patients will be carefully asked about their compliance with the treatment. Patients who interrupted the treatment for adverse events or low compliance (<75% of the protocol adherence) will exit the study and be excluded from the analysis.

At Visit 3, the study population will be evaluated as done in Visit 2

The protocols in the study are the following:

LCD (low-dose continuous protocol) - 50 mg of doxycycline for three months FPP ( Full-dose pulsed protocol) - 100 mg of doxycycline for the first 15 days of the month for three months.

The enrollment period will last about 6 months. Therefore, the study will end about 6 months after the last patient enrols.

Conditions

Meibomian Gland Dysfunction; Blepharitis; Doxycycline Adverse Reaction

Study Design

• Observational Model Type: COHORT
• Study Time Perspective: PROSPECTIVE

Study Groups

LCP - Low dose continuous protocol

Assumption of 50 mg of oral doxycycline per day for 3 months

Doxycyclin

Intervention Type: DRUG

The drug has been prescribed, as in normal clinical practice, with the National Healthcare System. Patients have been fully informed about interactions, toxicity and posology schedule.

FPP - Full dose pulsed protocol

Assumption of 100 mg of oral doxycycline per day for 15 days per month (with a subsequent 15 days of washout) for 3 months

Doxycyclin

Intervention Type: DRUG

The drug has been prescribed, as in normal clinical practice, with the National Healthcare System. Patients have been fully informed about interactions, toxicity and posology schedule.

Interventions

Doxycyclin

The drug has been prescribed, as in normal clinical practice, with the National Healthcare System. Patients have been fully informed about interactions, toxicity and posology schedule.

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• 18 years or older
• Provided written informed consent
• OSDI score of 13 or more at the baseline visit after at least two months of first-line therapy (artificial tears and warm compresses)
• Clinical diagnosis of MGD
• Type 1 Schirmer test > 10 mm
• No previous history of allergy or sensitivity to doxycycline,
• No use of additional topical or systemic antibiotics for the prior 2 months
• No use of topical anti-inflammatory agents (ex: corticosteroids or cyclosporine) for the prior 3 months.

Exclusion Criteria

• Active ocular inflammation in either eye,
• Demodex blepharitis,
• Ocular surgery within the past 3 months of baseline examination,
• Structural ocular surface and eyelid abnormalities.
• Sjögren's syndrome
• Rheumatoid arthritis
• Other systemic diseases resulting in dry eye
• Known autoimmune disease
• Doxycycline allergy or sensitivity
• History of antibiotic therapy at any time within 2 months of the commencement of study
• Use of significant calcium supplementation or other medications that could interfere with doxycycline absorption (es: Iron supplementation)

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 100 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

University of Milan

OTHER

Sponsor Role: lead

Responsible Party

Paolo Fogagnolo

Associate professor

Responsibility Role: PRINCIPAL_INVESTIGATOR

Locations

ASST Santi Paolo e Carlo - Ospedale San Paolo

Milan, MI, Italy

Countries

Italy

Provided Documents

Document Type: Study Protocol

View Document

Other Identifiers

CPDOXY1

Identifier Type: -

Identifier Source: org_study_id