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Dynamic Parameters of Glucose Control in Relation to Biomarkers in Serum and Intraocular Fluid in Patients With Diabetes

Recruiting
Conditions
Diabetes Complications
Interventions
Procedure: Intraocular surgery
Registration Number
NCT05944640
Lead Sponsor
Charles University, Czech Republic
Brief Summary

Our project investigates the new characteristics of diabetic retinopathy using liquid eye biopsy in combination with novel parameters of glucose control obtained with continuous glucose monitoring. This approach will bring new knowledge and implications for future therapies.

Detailed Description

Diabetic retinopathy is one of the most common causes of blindness in developed countries. The short-term glucose fluctuations have been suggested as a factor contributing to the risk of diabetic complications including ocular complications. We hypothesize that modulatory and other biological abilities of miRNAs and inflammatory chemokines/cytokines have a significant impact on the development and the progression of diabetic retinopathy. Our main goal is to identify the biomarkers that will in time be used for new screening, diagnostic, and treatment strategies for patients with diabetic retinopathy, bring a better prevention and early treatment to them and thus improve their quality of life while saving the cost associated with advanced forms of retinopathy.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
213
Inclusion Criteria
  • type 1 or type 2 diabetes
  • ≥ 18 years old
  • treatment with insulin for at least 5 years prior baseline
  • any form of diabetic retinopathy and macular edema
  • HbA1c < 10%
  • written informed consent prior to starting study related activity
Exclusion Criteria
  • any active intraocular or periocular infectious or non-infectious inflammation in study eye
  • uncontrolled glaucoma
  • history of intraocular inflammation or trauma in study eye
  • intravitreal anti-VEGF therapy in study eye during a 3-month perido prior to baseline
  • use of corticosteroid intravitreal implant in study eye at any time

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Control groupIntraocular surgerySubjects without diabetes mellitus indicated for ocular surgery from other reasons (cataract, retinal detachment, macular hole, idiopathic epiretinal membrane) as standard of care. Blood samples and samples of intraocular fluids will bee taken during the ocular surgery.
Patients with DRIntraocular surgeryAdult patients with T1DM or T2DM with any form of diabetic retinopathy and diabetic macular edema, indicated for ocular surgical procedure as standard of care. Blood samples and samples of intraocular fluids will bee taken during the ocular surgery.
Patients without DRIntraocular surgeryAdult patients with T1DM or T2DM without any signs of diabetic retinopathy, indicated for ocular surgical procedure from other reasons as standard of care. Blood samples and samples of intraocular fluids will bee taken during the ocular surgery.
Primary Outcome Measures
NameTimeMethod
TIRYear 2025

Percentage of time in target ranges

miRNAYear 2025

miRNA expression measuer by real-time PCR method in plasma and vitreous samples (units: threshold cycle)

Secondary Outcome Measures
NameTimeMethod
Glycemic variabilityYear 2025

Expressed as the standard deviation

Mean sensor glucose concentrationYear 2025

Measured by rtCGM

miRNA expression differencesYear 2025

miRNA expression differences analysis between diabetic patients with and without diabetic retinopathy (units: fold change)

Trial Locations

Locations (1)

General University Hospital in Prague

🇨🇿

Prague, Czechia

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