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Combined Antioxidant Therapy on Oxidative Stress in Aqueous and Vitreous Humor of Diabetic Retinopathy Patients

Primary Purpose

Diabetic Retinopathy, Oxidative Stress, Diabetes

Status
Completed
Phase
Phase 2
Locations
Mexico
Study Type
Interventional
Intervention
Combined antioxidant therapy
Placebo
Sponsored by
University of Guadalajara
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Diabetic Retinopathy focused on measuring Vitreous humor, Vitrectomy, Aqueous humor, Antioxidant therapy, Oxidative markers

Eligibility Criteria

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

Inclusion Criteria:

  • Patients with type 2 with proliferative diabetic retinopathy
  • Blood pressure under 160/100 mmHg
  • HbA1c equal or lower than 9%
  • LDL under 190mg/dl, triglycerides under 500mg/dl)
  • Signed informed consent
  • Patients scheduled for vitrectomy surgery, under the following indications:
  • Severe vitreous hemorrhage lasting 1-3 months or longer, which does not go away spontaneously
  • Rhegmatogenous or tensile retina detachment
  • Epiretinal membrane that involves macula and that includes vitreomacular traction

Exclusion Criteria:

  • Vitreous hemorrhage for any cause other than Proliferative Diabetic Retinopathy complication
  • Patients with vitrectomy surgery in the last 6 months
  • Patients with laser surgery in the last 6 months
  • Intravitreal application of antiangiogenic agents in the last 2 months
  • Patients with other ocular pathologies such as age-related macular degeneration, glaucoma, endophthalmitis, conjunctivitis of any etiology, severe lacrimal film dysfunction syndrome, etc.
  • Patients with concomitant systemic diseases such as: rheumatoid arthritis, sjogren's syndrome, upper respiratory tract infections, gastrointestinal infections, sepsis, any infectious process
  • Patients with severe cardiovascular disease (myocardial infarction, stroke, severe peripheral vascular disease)
  • Oral antioxidant intake that exceeds the daily recommendations in the last 6 months.
  • Consumption of pharmacological agents such as: immunomodulators, biological, anti-inflammatory, in the last 3 months
  • Smokers
  • Patients with neurodegenerative or carcinogen processes
  • Patients who are currently participating in other clinical trials

Sites / Locations

  • Institute of Experimental and Clinical Therapeutics,

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Combined Antioxidant Therapy group

Placebo group

Arm Description

This arm will be administered with the combined antioxidant therapy, and will consist of 28 patients with proliferative diabetic retinopathy (PDR) who will undergo vitrectomy.

This arm will be administered with placebo, and will consist of 28 patients with proliferative diabetic retinopathy (PDR) who will undergo vitrectomy.

Outcomes

Primary Outcome Measures

Compare levels of markers of oxidative stress in aqueous humor and vitreous humor
The investigators will measure oxidative stress markers in aqueous and vitreous humor taken during vitrectomy procedure and compare such results between both intervention groups.
Changes in concentration of plasma 8-isoprostanes after intervention.
The investigators will consider changes presented in plasma concentrations of 8-isoprostanes from baseline to the end of the intervention. The investigators expect to find a decrease in 8-isoprostanes concentrations in the supplemented group.
Changes in concentration of total antioxidant capacity (TAC) after intervention from baseline.
The investigators will consider changes presented in plasma concentrations of total antioxidant capacity (TAC) from baseline to the end of the intervention. The investigators expect to find TAC augmentation in the supplemented group.

Secondary Outcome Measures

Correlate the levels of 8-isoprostanes in systemic samples, aqueous humor and vitreous humor with the glycosylated hemoglobin value of patients with proliferative diabetic retinopathy.
The investigators will consider levels of 8-isoprostanes in serum, aqueous humor and vitreous humor after intervention and baseline glycated hemoglobin
Correlate the levels of total antioxidant capacity (TAC) in systemic samples, aqueous humor and vitreous humor with the glycosylated hemoglobin value of patients with proliferative diabetic retinopathy.
The investigators will consider levels of total antioxidant capacity in serum, aqueous humor and vitreous humor after intervention and baseline glycated hemoglobin

Full Information

First Posted
August 26, 2019
Last Updated
March 21, 2022
Sponsor
University of Guadalajara
Collaborators
Hospital Civil de Guadalajara
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1. Study Identification

Unique Protocol Identification Number
NCT04071977
Brief Title
Combined Antioxidant Therapy on Oxidative Stress in Aqueous and Vitreous Humor of Diabetic Retinopathy Patients
Official Title
Effect of Combined Antioxidant Therapy on the Levels of Oxidative Stress Markers in Aqueous and Vitreous Humor of Patients With Proliferative Diabetic Retinopathy
Study Type
Interventional

2. Study Status

Record Verification Date
March 2022
Overall Recruitment Status
Completed
Study Start Date
March 25, 2020 (Actual)
Primary Completion Date
October 31, 2021 (Actual)
Study Completion Date
December 31, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Guadalajara
Collaborators
Hospital Civil de Guadalajara

4. Oversight

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

5. Study Description

Brief Summary
The present study aims to support previous research on the effects of antioxidant therapy on the outcome of diabetic retinopathy and local oxidative stress values. The researchers intend to evaluate 56 patients with proliferative diabetic retinopathy undergoing the vitrectomy procedure, who will be assigned to a placebo group or combination antioxidant therapy. Each group will receive the intervention for 2 months. This intervention consists of taking one tablet (placebo or antioxidant therapy) orally, once a day. At the beginning of the study, only blood samples will be collected to evaluate the state of oxidative and metabolic stress at a systemic level. After 2 months of intervention, blood samples will be taken again on the day of the intervention, adding the samples of aqueous and vitreous humor obtained during the vitrectomy. The results obtained between both groups and the different analysis matrices will be compared.
Detailed Description
Diabetic retinopathy is a diabetes microvascular complication due to an insufficient oxygen supply to its endothelial cells in states of constant hyperglycemia. This entity is classified in two main categories: non-proliferative diabetic retinopathy and proliferative diabetic retinopathy, the latter is characterized for the presence of neovascularization as oppose to the first one. Oxidative stress has been considered as one of the main factors in the development of diabetic retinopathy. It is a result from an imbalance between oxidants production and cellular antioxidant defenses, which provokes DNA damage. The treatment of diabetic retinopathy simply includes glycemic, lipemic and blood pressure control. Only when the view is compromised is when a vitrectomy is performed, which usually occurs in the more advanced stages such as the proliferative stage. Antioxidant therapy has been used as a coadjuvant for these interventions, complementing the action and efficacy of the treatment established for diabetic retinopathy in the early stages. However, in order to obtain vitreous and aqueous humor, the vitrectomy procedure is required, which is only carried out in the proliferative stage. Diabetic retinopathy is a specific and chronic complication of diabetes mellitus and is known to have a prevalence of 43.6% internationally and 31.5% in the Mexican population. It represents the main cause of visual blindness and weakness in the economically active population, which also affects the quality of life and the productivity of the people who suffer it. The researchers intend to evaluate whether antioxidant therapy influences the levels of oxidative stress markers at the ocular level.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetic Retinopathy, Oxidative Stress, Diabetes
Keywords
Vitreous humor, Vitrectomy, Aqueous humor, Antioxidant therapy, Oxidative markers

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Model Description
Clinical trial phase IIa
Masking
ParticipantInvestigator
Masking Description
Drug
Allocation
Randomized
Enrollment
40 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Combined Antioxidant Therapy group
Arm Type
Active Comparator
Arm Description
This arm will be administered with the combined antioxidant therapy, and will consist of 28 patients with proliferative diabetic retinopathy (PDR) who will undergo vitrectomy.
Arm Title
Placebo group
Arm Type
Placebo Comparator
Arm Description
This arm will be administered with placebo, and will consist of 28 patients with proliferative diabetic retinopathy (PDR) who will undergo vitrectomy.
Intervention Type
Drug
Intervention Name(s)
Combined antioxidant therapy
Other Intervention Name(s)
Drusen Laz
Intervention Description
It consists of a tablet with lutein (10 mg), astaxanthin (4 mg), Zeaxanthin (1 mg), vitamin C (L-ascorbic acid 180 mg), vitamin E (DL-alpha tocopherol 30 mg), zinc (zinc oxide 20 mg), copper (copper sulfate 1 mg), taken once a day for 12 months
Intervention Type
Other
Intervention Name(s)
Placebo
Other Intervention Name(s)
Magnesia
Intervention Description
It consists in a capsule with 100 mg of magnesium oxide
Primary Outcome Measure Information:
Title
Compare levels of markers of oxidative stress in aqueous humor and vitreous humor
Description
The investigators will measure oxidative stress markers in aqueous and vitreous humor taken during vitrectomy procedure and compare such results between both intervention groups.
Time Frame
1 measure will be made after 2 months of intervention
Title
Changes in concentration of plasma 8-isoprostanes after intervention.
Description
The investigators will consider changes presented in plasma concentrations of 8-isoprostanes from baseline to the end of the intervention. The investigators expect to find a decrease in 8-isoprostanes concentrations in the supplemented group.
Time Frame
2 measures will be made, 1 at baseline, and one after completion of 2 months of intervention
Title
Changes in concentration of total antioxidant capacity (TAC) after intervention from baseline.
Description
The investigators will consider changes presented in plasma concentrations of total antioxidant capacity (TAC) from baseline to the end of the intervention. The investigators expect to find TAC augmentation in the supplemented group.
Time Frame
2 measures will be made, 1 at baseline, and one after completion of 2 months of intervention
Secondary Outcome Measure Information:
Title
Correlate the levels of 8-isoprostanes in systemic samples, aqueous humor and vitreous humor with the glycosylated hemoglobin value of patients with proliferative diabetic retinopathy.
Description
The investigators will consider levels of 8-isoprostanes in serum, aqueous humor and vitreous humor after intervention and baseline glycated hemoglobin
Time Frame
1 measure of glycated hemoglobin will be taken at baseline
Title
Correlate the levels of total antioxidant capacity (TAC) in systemic samples, aqueous humor and vitreous humor with the glycosylated hemoglobin value of patients with proliferative diabetic retinopathy.
Description
The investigators will consider levels of total antioxidant capacity in serum, aqueous humor and vitreous humor after intervention and baseline glycated hemoglobin
Time Frame
1 measure of glycated hemoglobin will be taken at baseline

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients with type 2 with proliferative diabetic retinopathy Blood pressure under 160/100 mmHg HbA1c equal or lower than 9% LDL under 190mg/dl, triglycerides under 500mg/dl) Signed informed consent Patients scheduled for vitrectomy surgery, under the following indications: Severe vitreous hemorrhage lasting 1-3 months or longer, which does not go away spontaneously Rhegmatogenous or tensile retina detachment Epiretinal membrane that involves macula and that includes vitreomacular traction Exclusion Criteria: Vitreous hemorrhage for any cause other than Proliferative Diabetic Retinopathy complication Patients with vitrectomy surgery in the last 6 months Patients with laser surgery in the last 6 months Intravitreal application of antiangiogenic agents in the last 2 months Patients with other ocular pathologies such as age-related macular degeneration, glaucoma, endophthalmitis, conjunctivitis of any etiology, severe lacrimal film dysfunction syndrome, etc. Patients with concomitant systemic diseases such as: rheumatoid arthritis, sjogren's syndrome, upper respiratory tract infections, gastrointestinal infections, sepsis, any infectious process Patients with severe cardiovascular disease (myocardial infarction, stroke, severe peripheral vascular disease) Oral antioxidant intake that exceeds the daily recommendations in the last 6 months. Consumption of pharmacological agents such as: immunomodulators, biological, anti-inflammatory, in the last 3 months Smokers Patients with neurodegenerative or carcinogen processes Patients who are currently participating in other clinical trials
Facility Information:
Facility Name
Institute of Experimental and Clinical Therapeutics,
City
Guadalajara
State/Province
Jalisco
ZIP/Postal Code
44340
Country
Mexico

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
23875878
Citation
Rodriguez-Carrizalez AD, Castellanos-Gonzalez JA, Martinez-Romero EC, Miller-Arrevillaga G, Villa-Hernandez D, Hernandez-Godinez PP, Ortiz GG, Pacheco-Moises FP, Cardona-Munoz EG, Miranda-Diaz AG. Oxidants, antioxidants and mitochondrial function in non-proliferative diabetic retinopathy. J Diabetes. 2014 Mar;6(2):167-75. doi: 10.1111/1753-0407.12076. Epub 2013 Aug 21.
Results Reference
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PubMed Identifier
26207797
Citation
Rodriguez-Carrizalez AD, Castellanos-Gonzalez JA, Martinez-Romero EC, Miller-Arrevillaga G, Roman-Pintos LM, Pacheco-Moises FP, Miranda-Diaz AG. The antioxidant effect of ubiquinone and combined therapy on mitochondrial function in blood cells in non-proliferative diabetic retinopathy: A randomized, double-blind, phase IIa, placebo-controlled study. Redox Rep. 2016 Jul;21(4):190-5. doi: 10.1179/1351000215Y.0000000032. Epub 2016 Feb 5.
Results Reference
background
PubMed Identifier
26321469
Citation
Rodriguez-Carrizalez AD, Castellanos-Gonzalez JA, Martinez-Romero EC, Miller-Arrevillaga G, Pacheco-Moises FP, Roman-Pintos LM, Miranda-Diaz AG. The effect of ubiquinone and combined antioxidant therapy on oxidative stress markers in non-proliferative diabetic retinopathy: A phase IIa, randomized, double-blind, and placebo-controlled study. Redox Rep. 2016 Jul;21(4):155-63. doi: 10.1179/1351000215Y.0000000040. Epub 2015 Aug 31.
Results Reference
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Citation
Sonia Sifuentes-Franco, Adolfo Daniel Rodríguez-Carrizalez, Sandra Carrillo- Ibarra, José Alberto Castellanos-González, Esaú César Martínez-Romero, Guillermo Miller-Arrevillaga and Alejandra Guillermina Miranda-Díaz. The effect of Ubiquinone administration on oxidative DNA damage and repair in plasma levels in non-proliferative diabetic retinopathy.Diabetes Management 2017;7(2):186-191
Results Reference
background
PubMed Identifier
31511825
Citation
Cecilia OM, Jose Alberto CG, Jose NP, Ernesto German CM, Ana Karen LC, Luis Miguel RP, Ricardo Raul RR, Adolfo Daniel RC. Oxidative Stress as the Main Target in Diabetic Retinopathy Pathophysiology. J Diabetes Res. 2019 Aug 14;2019:8562408. doi: 10.1155/2019/8562408. eCollection 2019.
Results Reference
background
PubMed Identifier
32256949
Citation
Robles-Rivera RR, Castellanos-Gonzalez JA, Olvera-Montano C, Flores-Martin RA, Lopez-Contreras AK, Arevalo-Simental DE, Cardona-Munoz EG, Roman-Pintos LM, Rodriguez-Carrizalez AD. Adjuvant Therapies in Diabetic Retinopathy as an Early Approach to Delay Its Progression: The Importance of Oxidative Stress and Inflammation. Oxid Med Cell Longev. 2020 Mar 11;2020:3096470. doi: 10.1155/2020/3096470. eCollection 2020.
Results Reference
background
PubMed Identifier
32962301
Citation
Lopez-Contreras AK, Martinez-Ruiz MG, Olvera-Montano C, Robles-Rivera RR, Arevalo-Simental DE, Castellanos-Gonzalez JA, Hernandez-Chavez A, Huerta-Olvera SG, Cardona-Munoz EG, Rodriguez-Carrizalez AD. Importance of the Use of Oxidative Stress Biomarkers and Inflammatory Profile in Aqueous and Vitreous Humor in Diabetic Retinopathy. Antioxidants (Basel). 2020 Sep 20;9(9):891. doi: 10.3390/antiox9090891.
Results Reference
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Combined Antioxidant Therapy on Oxidative Stress in Aqueous and Vitreous Humor of Diabetic Retinopathy Patients

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