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Metabolomic Profile in Dry Eye Syndrome Patients.

NCT05433428 · Status: UNKNOWN · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 250

Last updated 2022-06-27

No results posted yet for this study

Summary

The primary objective is to determine possible implications of deviant tear film quality for optimal refractive precision in patients scheduled for cataract surgery.

The study consist of three separate arms where cataract patients will be separated in to Dry Eye Disease (DED) positive and negative groups. The DED positive group will be further subdivided into two different treatment groups (with focus on prolonged use of lubricant and preservative free eye drops). Tear film samples will be taken before treatment, after treatment and after surgical treatment and compared.

Conditions

  • Dry Eye Syndromes
  • Cataract

Interventions

DRUG

Lubricant Eye Drops

Prolonged use of lubricant eye drops pre and post-op.

DRUG

Preservative Free

Preservative free eye drops

DRUG

Preservative

Eyedrops with preservatives

Sponsors & Collaborators

  • The Research Council of Norway

    collaborator OTHER

  • Ifocus Oyeklinikk

    lead NETWORK

Principal Investigators

  • Morten Gundersen, MD · IFocus Øyeklinikk AS

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
40 Years
Max Age
90 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2020-08-03
Primary Completion
2023-01-10
Completion
2023-05-23

Countries

  • Norway

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05433428 on ClinicalTrials.gov