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NCT ID: NCT06181227 Terminated - Clinical trials for Diabetic Retinopathy

A Phase 2 Study of Intravitreal AVD-104 in Diabetic Macular Edema

Start date: November 30, 2023
Phase: Phase 2
Study type: Interventional

A Phase 2 study to determine the safety and preliminary efficacy of intravitreal injections of AVD-104, a novel glyco-mimetic nanoparticle, in reducing macular edema associated with diabetic retinopathy.

NCT ID: NCT05079789 Terminated - Edema Clinical Trials

Amiloride in Nephrotic Syndrome

AMILOR
Start date: June 8, 2020
Phase: Phase 3
Study type: Interventional

The AMILOR study compares treatment of edema in nephrotic syndrome with Amiloride vs. Furosemide.

NCT ID: NCT05063734 Terminated - Diabetes Mellitus Clinical Trials

A Study to Evaluate THR-687 Treatment for Diabetic Macular Oedema.

INTEGRAL
Start date: August 27, 2021
Phase: Phase 2
Study type: Interventional

This study is conducted to select the THR-687 dose level (Part A of the study) and to assess the efficacy and safety of the selected dose level compared to aflibercept (Part B of the study).

NCT ID: NCT04991350 Terminated - Clinical trials for Diabetic Retinopathy

Effect of Ranibizumab Versus Bevacizumab on the Macular Perfusion in Diabetic Macular Edema

REBEL
Start date: November 26, 2021
Phase: Phase 4
Study type: Interventional

The Early Treatment Diabetic Retinopathy Study (ETDRS) group founded guidelines for treating patients with clinically significant diabetic macular edema (DME) with focal/grid macular laser photocoagulation. Since then, macular laser, and steroids, were the main therapies for the treatment of DME until anti-vascular endothelial growth factors (anti-VEGF) drugs were developed after a growing body of scientific evidence implicated VEGF in the pathophysiologic process of DME. Anti-VEGF drugs have been implicated in the treatment of DME. VEGF has been shown to play an important role in the occurrence of increased vascular permeability in DME. VEGF levels are significantly higher in patients with DME and extensive leakage than in patients with minimal leakage. Many studies such as Diabetic Retinopathy Clinical Research [DRCR] Network studies, RESTORE Study, RISE and RIDE Research Group, and The BOLT Study have supported the use of anti-VEGF agents in the treatment of DME with better visual outcomes using anti-VEGF injections alone or in combination with other treatments. Several ocular complications of intravitreal anti-VEGF injections have been reported including endophthalmitis, cataract, and retinal detachment. The different effects on macular perfusion between different anti-VEGFs have yet to be fully concluded with mixed conclusions that it increases or decreases or has no effect on perfusion of the macula in response to Anti-VEGF treatment. In many of these studies, however, patients with more ischemic retinas were not included. Retinal ischemia is a vital factor determining the diabetic retinopathy progression and prognosis. Optical coherence tomography angiography (OCTA) detects blood flow by analyzing signal decorrelation between two sequential OCT cross-sectional scans at the same location. As it detects the movements of red blood corpuscles within the vessels, compared to the stationary retinal surroundings, which will result in signal disparity and imaging The split-spectrum amplitude-decorrelation angiography (SSADA) algorithm improves the signal to noise ratio. OCTA is considered a reliable tool in the detection and quantification of macular ischemia in diabetics. In this study, the investigators aim to compare the effect of repeated intravitreal injections of ranibizumab and bevacizumab on the perfusion of different capillary layers in the macula of diabetic patients using OCTA.

NCT ID: NCT04712019 Terminated - Wounds and Injuries Clinical Trials

Evaluating Edema and Range of Motion Using Negative Pressure Therapy vs. Standard Surgical Dressing in Bilateral TKA

ENABLE
Start date: November 6, 2020
Phase: N/A
Study type: Interventional

This study will compare the effects of closed incision negative pressure dressing vs. standard of care silver dressing on lower limb swelling after bilateral primary total knee arthroplasty.

NCT ID: NCT04697758 Terminated - Clinical trials for Diabetic Macular Edema (DME)

Safety and Bioactivity of AXT107 in Subjects With Diabetic Macular Edema

CONGO
Start date: December 10, 2020
Phase: Phase 1/Phase 2
Study type: Interventional

This study is an open-label, dose-escalating, 48-week study assessing the safety, tolerability, bioactivity and duration of action of a single intravitreal injection of 0.1 mg, 0.25 mg, or 0.5 mg AXT107 in approximately 18 subjects (up to 6 subjects per dose) with Diabetic Macular Edema (DME).

NCT ID: NCT04611152 Terminated - Clinical trials for Diabetic Macular Edema

A Trial to Evaluate the Efficacy, Durability, and Safety of KSI-301 Compared to Aflibercept in Participants With Diabetic Macular Edema (DME)

GLEAM
Start date: September 30, 2020
Phase: Phase 3
Study type: Interventional

This Phase 3 study will evaluate the efficacy, durability, and safety of KSI-301 compared to aflibercept in participants with treatment-naïve DME.

NCT ID: NCT04603937 Terminated - Clinical trials for Diabetic Macular Edema

A Study to Evaluate the Efficacy, Durability, and Safety of KSI-301 Compared to Aflibercept in Participants With Diabetic Macular Edema (DME)

GLIMMER
Start date: September 30, 2020
Phase: Phase 3
Study type: Interventional

This Phase 3 study will evaluate the efficacy, durability, and safety of KSI-301 compared to aflibercept in participants with treatment-naïve DME.

NCT ID: NCT04296838 Terminated - Macular Edema Clinical Trials

Effects of Conbercept in Refractory Uveitic Macular Edema and VEGF

Start date: October 12, 2019
Phase: Phase 2/Phase 3
Study type: Interventional

As a primary exploratory study, this study aims to evaluate the short-term effectiveness of intravitreal Conbercept injection in UME, and to explore the correlation between inflammatory factors like VEGF and the responsiveness to treatment.

NCT ID: NCT03490916 Terminated - Clinical trials for High Altitude Pulmonary Edema

Effect of Acetazolamide on Subclinical High-Altitude Pulmonary Edema Detected by Lung Ultrasonography

Start date: March 23, 2018
Phase: Phase 4
Study type: Interventional

The overall goal of this study is to detect preclinical signs of HAPE by lung ultrasonography and evaluate the effectiveness of acetazolamide at decreasing pulmonary edema by using ultrasound.