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NCT06549023Recruiting

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

Single Session vs Multiple-Session Panretinal Photocoagulation With Navigated Laser in Proliferative Diabetic Retinopathy - The SMART-PRP Study

Source: ClinicalTrials.gov · Last updated 18 Nov 2025

Brief summary (registry, in English)

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.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
40 (estimated)
First submitted
8 Aug 2024
Start date
1 Jan 2025
Primary completion date
31 Dec 2028
Lead sponsor
Vastra Gotaland Region
NCT number
NCT06549023

What you commit to

  • Study type: Interventional
  • Planned participants: 40
  • From 1 Jan 2025 to the primary completion date, 31 Dec 2028
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • 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 study eye.
  • Treatment with medications known to risk macular edema.

Other illness

  • General medical condition making office laser treatment very difficult or impossible.

Other

  • Media opacity preventing adequate PRP.

Who the study is looking for

  • Age \> 18 years.
  • Patients with type 1 or type 2 Diabetes Mellitus with newly diagnosed Proliferative Diabetic Retinopathy, PDR.
  • Visual acuity ≥ 0.1 Snellen.
  • CRT of less than 300 micrometer measured by OCT without cysts in the neuroretina.
  • Clear media and adequately dilated pupil for PRP.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Ögonmottagning Mölndal/SU
Coordinator of this site? Confirm its status
MölndalSwedenRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.