CClinicalTrials.gg
Status unknownNCT01044875UMPDRUpdated Jan 8, 2010

Trial of Yellow 577 nm Laser Versus Green 532 nm Laser for Proliferative Diabetic Retinopathy

An interventional study of Pan retinal photocoagulation laser treatment in Proliferative Diabetic Retinopathy, sponsored by University of Malaya. Status unknown at 1 site in Malaysia. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2010-01-08.

Sponsored by University of Malaya · Not applicable, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Jan 2010), so the status shown — last known as Recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
120
Allocation
Randomized
Ages
18 Years and older
Sex
All
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Study summary

The purpose of this study is to measure effectiveness of yellow 577 nm laser compared to conventional green laser 532 nm for diabetic retinopathy in terms of number of treatment sessions required and visual acuity outcome.

The study also compares pain score of patients receiving laser treatment and side effects of laser treatment.

Read the detailed description

Diabetes mellitus (DM) is a major medical problem throughout the world. The most common and potentially most blinding of these complications is proliferative diabetic retinopathy (PDR).

Panretinal photocoagulation is established as the gold standard of treatment, supported by the data of the Diabetic Retinopathy Study (DRS).This study found that laser treatment reduced the rate of severe visual loss by 50%. Currently the green 532nm laser is the most common wavelength used. However, this conventional green laser has some complications such as pain, vitreous haemorrhage, choroidal effusion and visual field loss.

Due to the complication of conventional lasers, the yellow laser (577 nm)with peak absorption of oxyhemoglobin and good absorption of melanin is postulated to be more effective at producing retinal laser burns with a lower power and less pain compared to the green laser.

02

Conditions studied

  • Proliferative Diabetic Retinopathy

Keywords

  • Diabetic retinopathy
  • Laser treatment
  • Complications
  • Laser wavelength
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In context

Retinal Diseases

815 studies on the registry are indexed under Retinal Diseases; 105 are open to participants now.

This study's planned enrollment of 120 is above the median of 60 across 500 interventional studies indexed under Retinal Diseases.

Browse Retinal Diseases studies →

Lead sponsor

University of Malaya is the lead sponsor of 280 studies on the registry; 55 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Patient more than 18 year of age
  • Eyes with proliferative diabetic retinopathy requiring laser PRP
  • Newly diagnosed patient
  • Patients with no other intervention/surgeries done before the study

Exclusion criteria

Exclusion Criteria:

  • Eyes with media opacity not allowing adequate laser photocoagulation
  • Patients who have had previous laser photocoagulation
  • Patients who have had previous vitreoretinal surgery
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Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Investigator)
Enrollment
120 participants (estimated)

Study arms

  • Active comparator
    green laser 532 nm conventional

    Current type of laser used for treatment of proliferative diabetic retinopathy

    Procedure: Pan retinal photocoagulation laser treatment

  • Active comparator
    Yellow 577 nm laser

    new laser wavelength for treatment of PDR

    Procedure: Pan retinal photocoagulation laser treatment

Interventions

  • ProcedurePan retinal photocoagulation laser treatment

    Eyes with PDR are randomised to treatment with either the green laser 532 nm or 577 nm yellow laser.

    Also known as: Quantel Supra 577nm laser

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What researchers measure

Primary outcomes

  1. Visual acuity measurement by logarithm of the minimum angle of resolution (logMAR)

    Time frame: 2 years

Secondary outcomes

  1. Patient pain score during laser procedure

    Time frame: 2 years

07

Study locations

1 of 1 sites recruiting
  • University of Malaya Eye Research Centre
    Kuala Lumpur, 50603, Malaysia
    Recruiting
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 8, 2010, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT01044875
Lead sponsor
University of Malaya
First posted
Jan 8, 2010
Start date
Sep 2009
Primary completion
Sep 2011 (estimated)
Completion
Oct 2011 (estimated)
Last update
Jan 8, 2010

Study contacts

Thirupathy Annamalai, MBBS
Contact
thirusukan@yahoo.com
+79492060
Kenneth C Fong, FRCOphth
principal investigator · University of Malaya Eye Research Centre
Nurliza Khaliddin, FRCS
principal investigator · University of Malaya Eye Research Centre

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Jan 2010. You cannot join it, but the record below documents what was studied.

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