Effect of Lipid Based Eye Drops on Tear Film Lipid Layer Thickness

NCT03399292 | Completed

• 1 other identifier: OPHT-031116
• Study Type: observational
• Target: 12
• Locations: 1 country
• Sites: 1

Brief Summary

Dry eye disease (DED) is a common ocular disease, especially in the elderly population. Despite many treatment approaches, instillation of topical lubricants remains the mainstay of therapy. However, most of the topical lubricants available are not very well characterised and data about efficacy is sparse. The aim of the present pilot study is to investigate the effect of topically administered lipid based eye drops on tear film lipid layer thickness in subjects with dry eye disease, Meibomian gland dysfunction, blepharospasm and healthy subjects. Tear film lipid layer and tear film thickness will be assessed using the Lipiview II interferometer and OCT. Measurements will be performed before instillation of the eye drops and every 10 minutes after instillation for one hour. One eye will receive lipid based eye drops, the other eye will receive no eye drops and will be used as control. The study eye will be chosen randomly. In addition, Dynamic Meibomian gland imaging, Schirmer I test, corneal fluorescein staining and determination of tear break up time (BUT) will be performed

Conditions

Dry Eye Syndromes

Keywords

Lipid based eye drops; Tearfilm lipid layer thickness

Outcome Measures

Primary Outcomes (1)

• Tear film lipid layer thickness as measured with Lipiview II

  12.04.2017-30.12.2018

Study Arms (4)

Group 1

10 male and female healthy subjects receive Cationorm MD sine eye drops once

Drug: Cationorm MD sine eye drops

Group 2

10 male and female volunteers with dry eye disease receive Cationorm MD sine eye drops once

Drug: Cationorm MD sine eye drops

Group 3

10 male and female volunteers with Maibomian gland disease receive Cationorm MD sine eye drops once

Drug: Cationorm MD sine eye drops

Group 4

10 male and female volunteers with receive Cationorm MD sine eye drops once

Drug: Cationorm MD sine eye drops

Interventions

Cationorm MD sine eye drops DRUG

studyparticipants receive lipidbased eye drops once only in the study eye

Group 1; Group 2; Group 3; Group 4

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)
• Sampling Method: Probability Sample

Study Population

10 healthy male and female volunteers 10 male and female subjects with dry eye disease 10 male and female subjects with Meibomian gland dysfunction 10 male and female subjects with blepharospasm

You may qualify if:

• All groups
• Men and women aged over 18 years
• Normal findings in the medical history unless the investigator considers an abnormality to be clinically irrelevant
• Ametropy \< 6 dpt
• No application of eye drops or ointments in the 24 hours preceding the screening visit as well as the study day Dry eye disease group
• History of dry eye disease ≥ 3 months
• Schirmer I test ≤ 10 mm and ≥ 2 mm or BUT ≤ 10 sec
• Normal ophthalmic findings with the exception of DED Meibomian gland disease group
• Dry eye disease most likely caused by MGD, no other cause identifiable which is more likely (e.g. intake of concomitant medication that could induce DED, systemic diseases such as systemic arthritis or diabetes), as judged by the investigator
• History of dry eye disease ≥ 3 months
• Normal ophthalmic findings except dry eye disease
• BUT ≤ 10 seconds Blepharospasm group
• Clinical diagnosis of blepharospasm
• Normal ophthalmic findings with the exception of blepharospasm and dry eye
• Schirmer I test \> 10 mm and BUT \> 10 sec

You may not qualify if:

• All groups
• Clinically relevant illness in the 3 weeks before the screening or study day
• Ametropy ≥ 6 dpt
• Pregnancy or planned pregnancy
• Difference of more than 5 mm in Schirmer I test or difference of \> 3 sec in BUT between the two eyes
• Known medical history of allergy, hypersensitivity or poor tolerance to any components of the medical device used in the study
• Treatment with topical or systemic steroids, immune suppressants, NSAIDs: ongoing or in the last 4 weeks
• Treatment with medication known to have a detrimental effect on tear film (e.g. antidepressants, anxiolytics, neuroleptics, antihistaminic drugs, cholinergic drugs, antimuscarinic drugs, phenothiazine, beta blockers): treatment duration ≤ 4 weeks or changed dose since ≤ 4 weeks or during the study
• Alcohol abuse
• Contact lens wear Meibomian gland dysfunction group
• Sjögren's syndrome

Sponsors & Collaborators

• Medical University of Vienna: lead

Study Sites (1)

Department of Clinical Pharmacology, Medical University of Vienna

Vienna, Vienna, 1090, Austria

Location

MeSH Terms

Conditions

Dry Eye Syndromes

Condition Hierarchy (Ancestors)

Lacrimal Apparatus Diseases; Eye Diseases

Study Design

• Study Type: observational
• Observational Model: COHORT
• Time Perspective: PROSPECTIVE
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Assoc.Prof.PD MD

Study Record Dates

• First Submitted: January 8, 2018
• First Posted: January 16, 2018
• Study Start: April 12, 2017
• Primary Completion: November 26, 2024
• Study Completion: November 26, 2024
• Last Updated: May 23, 2025

Record last verified: 2022-04

Data Sharing

• IPD Sharing: Will not share

Locations

AU (1)