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Search / Trial NCT06549023

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

Launched by VASTRA GOTALAND REGION · Aug 8, 2024

Trial Information

Current as of June 26, 2025

Recruiting

Keywords

Panretinal Photocoagulation (Prp) Single Session Prp Multiple Session Prp Navigated Laser Navilas Central Subfield Retinal Thickness (Crt) Macular Volume Optical Coherence Tomography (Oct) Swept Source Optical Coherence Tomography (Ss Oct) Wide Field Fundus Imaging Oct Angiography Retinal Oximetry Electroretinogram (Erg)

ClinConnect Summary

This clinical trial is looking at two different ways to treat a serious eye condition called proliferative diabetic retinopathy (PDR), which can lead to blindness in people with diabetes. Researchers want to find out if it's better to have one treatment session or multiple sessions of a procedure called panretinal photocoagulation (PRP). This treatment helps to stop the growth of abnormal blood vessels in the eye that can cause vision problems.

To participate in this study, you need to be at least 18 years old and have type 1 or type 2 diabetes with newly diagnosed PDR. Your vision must be good enough for the treatment, and your eye needs to be in good condition for the procedure. If you’ve had recent eye surgeries or certain other eye conditions, you might not qualify. If you do participate, you can expect to receive either the single-session or multiple-session treatment and help researchers understand which method works better for patients like you. The study is currently recruiting participants, and everyone is welcome, regardless of gender.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • 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.
  • Exclusion Criteria:
  • 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.
  • Media opacity preventing adequate PRP.
  • General medical condition making office laser treatment very difficult or impossible.

About Vastra Gotaland Region

Vastra Gotaland Region is a prominent healthcare organization in Sweden, dedicated to advancing medical research and improving patient care through innovative clinical trials. As a sponsor, the region leverages its extensive network of hospitals and healthcare professionals to facilitate high-quality research initiatives that address pressing health challenges. With a commitment to ethical standards and patient safety, Vastra Gotaland Region strives to foster collaboration between researchers, clinicians, and patients, ensuring that clinical trials contribute valuable insights and advancements in medical science.

Locations

Mölndal, , Sweden

Patients applied

0 patients applied

Trial Officials

Marita Andersson Grönlund, M.D. Prof

Principal Investigator

Göteborg University

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported