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Supplementation With a Highly-Concentrated Docosahexaenoic Acid (DHA) Triglyceride in Patients With Keratoconus

Primary Purpose

Keratoconus

Status
Completed
Phase
Not Applicable
Locations
Spain
Study Type
Interventional
Intervention
Highly-concentrated DHA triglyceride (Tridocosahexanoin-AOX 70%)
Sponsored by
Fundación para el Fomento de la Investigación Sanitaria y Biomédica de la Comunitat Valenciana
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Keratoconus

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Diagnosis of keratoconus stages I to III according to the Amsler-Krumeich classification Non-contact lens wearers No history of previous corneal surgery Capacity to volunteer and willing and able to follow the study protocol Exclusion Criteria: Advanced keratoconus (stage IV of the Amsler-Krumeich classification Other ectasias (e.g. iatrogenic secondary to ocular surface surgery with excimer laser, radial keratotomy, traumatic corneal ectasia, etc.) Eyelid alterations Previous ocular surgery Any ocular or systemic condition that may affect the interpretation of results Glaucoma or ocular hypertension History of ocular trauma, infection or inflammation Current treatment with topical or anti-inflammatory drugs Use of nutritional supplements including omega-3 fatty acids, vitamins and minerals (unless a washout period of 1 month had been established) Hypersensitivity to fish proteins Pregnant women Refusal to sign the written informed consent

Sites / Locations

  • FISABIO Medical Ophthalmology (FOM)

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

DHA group

Control group

Arm Description

Supplementation with a highly-concentrated docosahexaenoic acid (DHA) triglyceride (1000 g/day) for 3 months

Routine care

Outcomes

Primary Outcome Measures

Corneal topography
Changes of ophthalmological parameters
Antioxidant variables
Changes in plasma total antioxidant capacity (TAC), malondialdehyde (MDA) and glutathione (GSH), and GSH/GSSH ratio
Anti-inflammatory variables
cytokine levels IL-1beta, IL-4, IL-6, IL-10, IL-18, TNFalpha, VEGF-A

Secondary Outcome Measures

Lipidomic variables
Serum levels of DHA, arachidonic acid (ARA), n-6 PUFA/n-3 PUFA, omega-3 index

Full Information

First Posted
February 9, 2023
Last Updated
February 23, 2023
Sponsor
Fundación para el Fomento de la Investigación Sanitaria y Biomédica de la Comunitat Valenciana
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1. Study Identification

Unique Protocol Identification Number
NCT05756062
Brief Title
Supplementation With a Highly-Concentrated Docosahexaenoic Acid (DHA) Triglyceride in Patients With Keratoconus
Official Title
Antioxidant and Anti-inflammatory Effects of Oral Supplementation With a Highly-Concentrated Docosahexaenoic Acid (DHA) Triglyceride in Patients With Keratoconus: A Randomized Controlled Preliminary Study
Study Type
Interventional

2. Study Status

Record Verification Date
February 2023
Overall Recruitment Status
Completed
Study Start Date
February 1, 2019 (Actual)
Primary Completion Date
January 10, 2022 (Actual)
Study Completion Date
January 10, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Fundación para el Fomento de la Investigación Sanitaria y Biomédica de la Comunitat Valenciana

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The goal of this randomized controlled preliminary study is to assess the effect of daily supplementation with a nutraceutical formulation of a highly-concentrated DHA triglyceride plus minerals on ophthalmological parameters and biomarkers of oxidative stress and inflammation in blood samples of patients with keratoconus.The main questions it aims to answer are: Improvements in ophthalmological parameters. Increase in antioxidant capacity, decrease in inflammatory status, and changes in lipidomic biomarkers. Participants are patients with keratoconus who will be given the nutraceutical supplementation for 3 months. If there is a comparison group: Researchers will compare patients with keratoconus not given the nutraceutical formulation to see differences in the study variables
Detailed Description
Among omega-3 polyunsaturated fatty acids (PUFAs), docosahexaenoic acid (DHA, C22:6-n3), a critical component of cell membrane phospholipids, exerts pleiotropic effects at both central and peripheral levels with health benefits in many aspects of neuronal, immune, cognitive, and cardiovascular functions Clinical studies of dietary sup-plementation with a highly-concentrated DHA triglyceride have shown consistent an-ti-inflammatory, antioxidant, antiangiogenic, and antiproliferative effects targeting pathophysiological pathways involved in different eye diseases, including diabetic retinopathy and macular edema, ocular surface disorders, meibomian gland dysfuncton, and pseudoexfoliative glaucoma. Based on this experience, it was considered of interest to explore the antioxidant and anti-inflammatory potential of a highly-concentrated DHA triglyceride supplement in patients with keratoconus. For this purpose, a prospective preliminary study was designed to assess the effects of 3-month DHA nutritional supplementation on clinical variables, and inflammatory and oxidative stress biomarkers of patients with early and moderate keratoconus.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Keratoconus

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
34 (Actual)

8. Arms, Groups, and Interventions

Arm Title
DHA group
Arm Type
Experimental
Arm Description
Supplementation with a highly-concentrated docosahexaenoic acid (DHA) triglyceride (1000 g/day) for 3 months
Arm Title
Control group
Arm Type
No Intervention
Arm Description
Routine care
Intervention Type
Dietary Supplement
Intervention Name(s)
Highly-concentrated DHA triglyceride (Tridocosahexanoin-AOX 70%)
Intervention Description
Daily administration of 2 capsules of the study product (1000 mg DHA triglyceride) for 3 months
Primary Outcome Measure Information:
Title
Corneal topography
Description
Changes of ophthalmological parameters
Time Frame
Baseline and after 3 months of supplementation (end of study)
Title
Antioxidant variables
Description
Changes in plasma total antioxidant capacity (TAC), malondialdehyde (MDA) and glutathione (GSH), and GSH/GSSH ratio
Time Frame
Baseline and after 3 months of supplementation (end of study)
Title
Anti-inflammatory variables
Description
cytokine levels IL-1beta, IL-4, IL-6, IL-10, IL-18, TNFalpha, VEGF-A
Time Frame
Baseline and after 3 months of supplementation (end of study)
Secondary Outcome Measure Information:
Title
Lipidomic variables
Description
Serum levels of DHA, arachidonic acid (ARA), n-6 PUFA/n-3 PUFA, omega-3 index
Time Frame
Baseline and after 3 months of supplementation (end of study)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Diagnosis of keratoconus stages I to III according to the Amsler-Krumeich classification Non-contact lens wearers No history of previous corneal surgery Capacity to volunteer and willing and able to follow the study protocol Exclusion Criteria: Advanced keratoconus (stage IV of the Amsler-Krumeich classification Other ectasias (e.g. iatrogenic secondary to ocular surface surgery with excimer laser, radial keratotomy, traumatic corneal ectasia, etc.) Eyelid alterations Previous ocular surgery Any ocular or systemic condition that may affect the interpretation of results Glaucoma or ocular hypertension History of ocular trauma, infection or inflammation Current treatment with topical or anti-inflammatory drugs Use of nutritional supplements including omega-3 fatty acids, vitamins and minerals (unless a washout period of 1 month had been established) Hypersensitivity to fish proteins Pregnant women Refusal to sign the written informed consent
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Cristina Peris-Martinez, MD
Organizational Affiliation
FISABIO Medical Ophthalmology (FOM)
Official's Role
Principal Investigator
Facility Information:
Facility Name
FISABIO Medical Ophthalmology (FOM)
City
Valencia
ZIP/Postal Code
46015
Country
Spain

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Supplementation With a Highly-Concentrated Docosahexaenoic Acid (DHA) Triglyceride in Patients With Keratoconus

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