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Pattern Scanning Laser Pan-retinal Photocoagulation in Proliferative Diabetic Retinopathy

U

United Christian Hospital

Status

Completed

Conditions

Lasers
Treatment Outcome
Diabetic Retinopathy

Treatments

Device: Pan-retinal photocoagulation using pattern scanning laser

Study type

Interventional

Funder types

Other

Identifiers

NCT02816073
12-0079

Details and patient eligibility

About

A randomized study to assess the safety and efficacy of single-session pan-retinal photocoagulation (PRP) using Pattern Scan Laser (PASCAL) in proliferative diabetic retinopathy (PDR) - 1,700 shots vs 2,500 shots

Enrollment

17 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • All treatment-naïve patients with proliferative diabetic retinopathy (PDR) who attended our ophthalmic clinic from 1st December 2012 to 30th November

Exclusion criteria

  • significant media opacity affecting laser uptake (e.g. corneal opacity, mature cataract, dense vitreous haemorrhage)
  • any pre-existing ocular disorders resulting in visual impairment (e.g. retinal degenerations, maculopathies, primary glaucoma and other optic neuropathies)
  • those who received previous retinal laser treatment, intravitreal injections or intraocular surgeries
  • clinically significant macular oedema on clinical examination.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

17 participants in 2 patient groups

1,700
Active Comparator group
Description:
Patients receive 1,700 (+/- 5%) laser shots in a single session of pan-retinal photocoagulation using pattern scanning laser
Treatment:
Device: Pan-retinal photocoagulation using pattern scanning laser
2,500
Active Comparator group
Description:
Patients receive 2,500 (+/- 5%) laser shots in a single session of pan-retinal photocoagulation using pattern scanning laser
Treatment:
Device: Pan-retinal photocoagulation using pattern scanning laser

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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