DME

7

Review clinical trials related to DME. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

COMO: A Phase 3 Randomized, Double-Masked Study Comparing the Efficacy of EYP-1901 Against Aflibercept in DME

This is a phase 3 randomized, double -masked study comparing the efficacy of EYP-1901 against Aflibercept.

Participants needed: 240
Trial details
Phase: Phase 3Age: 18+Biological sex: AllType: InterventionalSponsor: EyePoint Pharmaceuticals, Inc.Updated: Jun 3, 2026Locations: 65
Eligibility criteria

Previously treated or treatment naïve patients with a documented diagnosis of ma... [+2]

BCVA using ETDRS charts <30 letters (20/250 Snellen equivalent) in the fellow ey...

Status: Recruiting

CAPRI: A Phase 3 Randomized, Double-Masked Study Comparing the Efficacy of EYP-1901 Against Aflibercept in DME

This is a phase 3 randomized, double -masked study comparing the efficacy of EYP-1901 against Aflibercept.

Participants needed: 240
Trial details
Phase: Phase 3Age: 18+Biological sex: AllType: InterventionalSponsor: EyePoint Pharmaceuticals, Inc.Updated: Jun 3, 2026Locations: 62
Eligibility criteria

Previously treated or treatment naïve patients with a documented diagnosis of ma... [+2]

BCVA using ETDRS charts <30 letters (20/250 Snellen equivalent) in the fellow ey...

Status: Not yet recruiting

AI vs. Physician for Anti-VEGF Decision-Making: An RCT

We developed an artificial intelligence system, called QiLin, which was designed to assist anti-VEGF treatment decisions in retinal diseases. QiLin was trained and validated via over 20,000 optical coherence tomography images from multicenter datasets, demonstrating strong performance on both internal and external validation. To evaluate its real-world clinical utility, we conducted a randomized controlled trial that rigorously compares the accuracy of treatment decisions between a physician-only arm and an AI-assisted physician arm.

Participants needed: 200
Trial details
Age: 50-85Biological sex: AllType: InterventionalSponsor: Shanghai General Hospital, Shanghai Jiao Tong University School of MedicineUpdated: May 22, 2026Locations: 2
Eligibility criteria

Not listed

Status: Not yet recruiting

Study of CU06-1004 in Patients With Daibetic Macular Edema

This phase 2b trial is a randomized, double-masked, parallel-group, multi-center study in approximately 156 patients with DME to evaluate the efficacy and safety of CU06-1004 orally administered once daily for 24 weeks. The study will have a 1:1:1 randomization (CU06-1004 200mg: CU06-1004 300mg: Placebo).

Participants needed: 156
Trial details
Phase: Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: Curacle Co., Ltd.Updated: Mar 10, 2026
Eligibility criteria

Have read, understood, and signed the informed consent form. [+9]

Has only 1 functional eye, even if the eye met all other study requirements, or... [+36]

Status: Not yet recruiting

The Effect of Bulk Filling Flowable Composite on Caries Recurrence in Deep Marginal Elevation: A Randomized Clinical Trial

Deep marginal elevation usinge a bioactive dental material in deep subgingival Class II restorations, S-PRG filler-containing materials offer significant benefits due to their bioactive properties, Their ability to release fluoride, remineralization potential and acid neutralization, reducing the risk of recurrent caries, particularly at the gingival margin(Imazato et al. 2023). The antibacterial and antifungal effects help inhibit biofilm formation, enhancing the longevity of restorations. Additionally, these materials support better marginal adaptation by reducing microleakage and improving bond durability (Imazato et al. 2023) This type of composite may improve the outcomes of deep subgingival margin elevation, benefiting both restorative success and periodontal health(Imazato et al. 2023).

Participants needed: 50
Trial details
Age: 20-50Biological sex: AllType: InterventionalSponsor: Future University in EgyptUpdated: Mar 28, 2025
Eligibility criteria

Adults patients (20-50) [+7]

• Patients with known allergic or adverse reaction to the tested materials. [+6]

Status: Not yet recruiting

Clinical Performance of High Viscosity Bioactive Injectable Composite in Deep Marginal Elevation

Using a bioactive resin composite in subgingival Class II cavities can provide enhanced caries resistance by releasing multiple ions, including fluoride. This approach offers greater resistance to caries due to the incorporation of surface pre-reacted glass filler (S-PRG) technology (Imazato, Nakatsuka et al., 2023). This type of composite may improve the outcomes of deep subgingival margin elevation, benefiting both restorative success and periodontal health.

Participants needed: 50
Trial details
Age: 20-50Biological sex: AllType: InterventionalSponsor: Future University in EgyptUpdated: Mar 13, 2025
Eligibility criteria

Adult Patient (20-50 years old) [+6]

Patients with known allergic or adverse reaction to the tested materials. [+6]