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A clinical study to evaluate effect and safety of NTGX-10 in treatment of patients with Diabetic Retinopathy

Not Applicable
Conditions
Health Condition 1: E103- Type 1 diabetes mellitus with ophthalmic complicationsHealth Condition 2: E113- Type 2 diabetes mellitus with ophthalmic complications
Registration Number
CTRI/2019/05/018928
Lead Sponsor
Rasayani Biologics Pvt Ltd Pune
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Open to Recruitment
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1 Type 1 or Type 2 diabetes mellitus

2 18 years or older

3 Patients of NPDR DME and PDR defined as follows

4 Severe non-proliferative diabetic retinopathy NPDR four-quadrant haemorrhage two-quadrant venous beading or one-quadrant based on the 4:2:1 rule intraretinal microvascular abnormalities

5 Diabetic macular oedema Haemorrhage microaneurysms exudates or thickening within one disk diameter of the fovea, or unexplained visual acuity loss

6 Proliferative diabetic retinopathy PDR Formation of new blood vessels

Exclusion Criteria

1 Presence of eye disorders other than diabetic retinopathy that may affect the progression of diabetic retinopathy or cause vision loss.

2 Patients who are allergic to Fluorescent sodium.

3 Patients with Glaucoma

4 Presence of central cataract

5 Patients with vitreous Haemorrhage

6 Presence of severe unstable angina pectoris

7 Presence of malignancy

8 Patient receiving Anti VEGF therapy or received in last 2 months

9 Severe uncontrolled Diabetes as determined by HbA1c >= 13.0%

10 Patients of severe uncontrolled hypertension as defined by systolic BP > 170 mm/hg

11 Presence of any other illness which in the opinion of Investigator will confound with the outcomes of the study or will adversely affect the study participation.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The primary objective of the study is to evaluate change in best corrected visual acuity.Timepoint: Monthly Interval for 6 months
Secondary Outcome Measures
NameTimeMethod
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