Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06549023

Single Session vs Multiple-Session Panretinal Photocoagulation for Treatment of Proliferative Diabetic Retinopathy

Led by Vastra Gotaland Region · Updated on 2025-11-18

40

Participants Needed

1

Research Sites

312 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Proliferative diabetic retinopathy (PDR) is the leading cause for blindness in working-age adults. The current gold standard treatment for PDR is panretinal photocoagulation (PRP). In current clinical practice, both single-session and multiple-session PRP approaches are widely accepted and utilized. The purpose of this study is to compare the safety and effectiveness of single-session and multiple-session PRP.

CONDITIONS

Official Title

Single Session vs Multiple-Session Panretinal Photocoagulation for Treatment of Proliferative Diabetic Retinopathy

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age > 18 years
  • Patients with type 1 or type 2 Diabetes Mellitus with newly diagnosed Proliferative Diabetic Retinopathy (PDR)
  • Visual acuity ≥ 0.1 Snellen
  • Central retinal thickness (CRT) less than 300 micrometers measured by OCT without cysts in the neuroretina
  • Clear media and adequately dilated pupil for panretinal photocoagulation (PRP)
Not Eligible

You will not qualify if you...

  • Intraocular surgery within the last 4 months or planned within the next 3 months
  • Previous or current center-involved diabetic macular edema (Ci-DME)
  • Previous PRP, intravitreal treatment (IVT), or macular laser treatment in the study eye
  • Treatment with medications known to increase risk of macular edema
  • Media opacity preventing adequate PRP
  • General medical condition making office laser treatment very difficult or impossible

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Ögonmottagning Mölndal/SU

Mölndal, Sweden, 43130

Actively Recruiting

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Research Team

I

Imadeddin Abu Ishkheidem, M.D.

CONTACT

S

Sofia Töyrä Silfverswärd, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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