- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06351033
Ozonized Oil as Dietary Supplement in Macular Degeneration
Efficacy of Ozonated Oil as a Dietary Supplement in the Clinical Management of Patients With Macular Degeneration
Macular degeneration, also called age-related macular degeneration (AMD), is a leading cause of visual impairment and severe vision loss.
AMD is a disease with a multifactorial etiology. The main factors which, associated with the genetic ones, increase the risk of WMD onset are represented by smoking, obesity, hypertension, cardio-vascular diseases, a diet rich in dietary fat and alcohol intake. From an organic point of view, AMD is a disease that affects the macular region of the retina, causing progressive loss of central vision.
Retinal cells are characterized by high oxygen consumption. Reactive oxygen species (ROS), such as superoxide anion, hydrogen peroxide and hydroxyl radical are the standard product of cellular metabolism within the mitochondria. Under physiological conditions, ROS are neutralized by a system of antioxidants. In case of cellular metabolism disturbances or insufficiency of the antioxidant system, an excess of ROS can be produced which contributes to oxidative stress, widely described as exerting deleterious effects on cells. The high oxygen requirement and low levels of antioxidant enzymes make the retina extremely sensitive to oxidative stress and more susceptible to cell death. Prevention of neuronal death in the retina becomes a crucial aspect for the management of WMD.
The treatment of choice for AMD today is the use of anti-VEGF (Vascular Endothelial Growth Factor) drugs, they are effective for neo-vascular AMD, acting on the inhibition of the angiogenic protein VEGF, which is produced in the retina and induced by hypoxia and other conditions. It is practice, however, to support the integration of nutritional supplements such as zinc, resveratrol, carotenoids such as lutein and zeaxanthin, vitamin E and Omega-3 fatty acids.
The aim of this study is to evaluate the efficacy of ozonated oil with high ozonides (HOO) administered orally as gastro-resistant capsules (O3Zone, GS Pharma, Malta), as an integrative and complementary treatment in patients affected by macular degeneration in the possible slowing of disease progression.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The aim of the study is to evaluate the efficacy of ozonated oil with high ozonides (HOO) administered orally as gastro-resistant capsules (O3Zone, GS Pharma, Malta), as an integrative and complementary treatment in patients affected by macular degeneration.
Field of view will be monitored to reveal the possible slowing of disease progression.
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Locations
-
-
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Pozzilli, Italy
- IRCCS Neuromed
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Definite AMD diagnosis with documented disease progression within the past 6 months
- Age: 50-85 years old
- Ascertained differential diagnosis with the aid of diagnostic tools: fundus examination eye; analysis of the macular region using optical computed tomography (OCT)
Exclusion Criteria:
- Psychiatric diseases
- Type I and II diabetes
- Patients with high refractive defects: myopia > 6 d; hyperopia > 4 d; astigmatism > 4 d
- Corneal pathologies
- Hereditary retinal diseases
- Autoimmune diseases (uveitis)
- Glaucoma
- Oncological diseases
- Liver and kidney disease
- Inclusion in other clinical trials
- Inability to understand informed consent and the purpose of the study
- Women who are pregnant or who may become pregnant during treatment
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Placebo
Placebo: control group made up of subjects affected by maculopathy - eligible according to the study protocol - subjected to traditional elective treatments only (including intravitreal Anti-VEGF injections).
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|
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Ozonized Oil
Ozonized Oil: intervention group made up of subjects affected by maculopathy - eligible according to the study protocol - subjected to the traditional treatments of choice (including anti-VEGF intravitreal injections) who receive supplementary treatment with the intake of HOO gastro-resistant capsules.
|
ozonated oil with high ozonides (HOO) administered orally (os) in gastro-resistant capsules
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
evaluation of any slowing down of the maculopathy
Time Frame: 3 months from the beginning of the ozonated oil administration
|
field of view
|
3 months from the beginning of the ozonated oil administration
|
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evaluation of any slowing down of the maculopathy
Time Frame: 6 months from the beginning of the ozonated oil administration
|
field of view
|
6 months from the beginning of the ozonated oil administration
|
|
evaluation of any slowing down of the maculopathy
Time Frame: 9 months from the beginning of the ozonated oil administration
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field of view
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9 months from the beginning of the ozonated oil administration
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evaluation of any slowing down of the maculopathy and closure of the study
Time Frame: 12 months from the beginning of the ozonated oil administration
|
field of view
|
12 months from the beginning of the ozonated oil administration
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Eliana Palermo, IRCCS Neuromed
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- ADP_012023
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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