Navigation Laser Versus Traditional Laser Photocoagulation for Mild Diabetic Macular Edema

Sponsor
Sun Yat-sen University (Other)
Overall Status
Unknown status
CT.gov ID
NCT03641144
Collaborator
(none)
80
1
2
18
4.4

Study Details

Study Description

Brief Summary

The aim of this study is to evaluate treatment effect and safety of navigation laser photocoagulation for mild diabetic macular edema compared with traditional laser.

Condition or Disease Intervention/Treatment Phase
  • Device: Navigation laser
  • Device: Traditional laser
N/A

Detailed Description

navigation laser is a novel fundus imaging and laser treatment method that allows imaging (infrared, colour, fluorescein angiography) and integrated laser treatment of the retina. Besides documentation, precision,safety and patient comfort,the main theoretical advantages lie in retina navigation.This randomized, parallel controlled, clinical-trial aims to evaluate treatment effect and safety of navigation laser photocoagulation for mild diabetic macular edema compared with traditional laser. The primary outcome measures is the Best-corrected visual acuity (BCVA) of the participants at 1 year after treatment. Besides, the slit-lamp examination, tonometry, funduscopy, and OCT, FFA, ICGA examinations will also be compared between different groups to find the advantage of navigation laser .

Study Design

Study Type:
Interventional
Anticipated Enrollment :
80 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Participant, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Navigation Laser Versus Traditional Laser Photocoagulation for Mild Diabetic Macular Edema:A Prospective, Randomized, Paralleled Clinical Trial
Actual Study Start Date :
Jun 1, 2018
Anticipated Primary Completion Date :
Jul 1, 2019
Anticipated Study Completion Date :
Dec 1, 2019

Arms and Interventions

Arm Intervention/Treatment
Experimental: Navigation laser

Navigation laser photocoagulation treatment to the macular area of retinal thickening with a focal pattern and/or grid pattern

Device: Navigation laser
Navigation laser device is a scanning slit-based instrument.before treatment the surgeon plan laser spots on the screen based on image(infrared, colour, fluorescein angiography)and then apply automated patterns and single spots as appropriate.the device will automatically carry out the plan.
Other Names:
  • Navigation laser photocoagulation treatment
  • Active Comparator: Traditional laser

    Traditional laser photocoagulation treatment to the macular area of retinal thickening with a focal pattern and/or grid pattern

    Device: Traditional laser
    Traditional laser is a slitlamp based instrument.Surgeon operate traditional laer device while watching Participant's image(infrared, colour, fluorescein angiography) and then manually aim at and trigger laser.
    Other Names:
  • Traditional laser photocoagulation treatment
  • Outcome Measures

    Primary Outcome Measures

    1. Best corrected visual acuity [12 months]

      Best Corrected Visual Acuity will be measured by standard Early Treatment Diabetic Retinopathy Study (ETDRS) protocol

    Secondary Outcome Measures

    1. Central Retinal Thickness [12 months]

      Central Retinal Thickness will be performed by optical coherence tomography(OCT)

    2. 10°retinal sensitivity [12 months]

      Retinal sensitivity will be measured by microperimetry

    3. treatment time [1 hour]

      treatment time is time from laser treatment beginning to end

    4. Participants pain intensity [1 hour]

      Participants pain intensity will be immediately measured by Visual Analogue Scale/Score (VAS)after treatment.The VAS is a straight horizontal line of fixed length(100 mm). The ends are defined as the extreme limits of the parameter to be measured (pain) orientated from the left (0) to the right (100).The patient marks on the line the point that participants feel represents their perception of their current pain intensity.the VAS score is determined by measuring the distance (mm) on the 100mm line between the "0" anchor and the patient's mark, providing a range of scores from 0-100. A higher score indicates greater pain intensity.the following cut points on the pain VAS have been recommended: no pain (0-4 mm), mild pain(5-44 mm), moderate pain (45-74 mm), and severe pain (75-100 mm) .

    5. Number of laser spots within macular fovea [1 month]

      Number of laser spots within macular fovea will measured by foundus photograph

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 80 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Aged ≥18 years

    • Diagnosed as diabetic retinopathy with Mild macular edema

    • BCVA≥0.5

    • No macular laser coagulation or surgery or medicine therapy of macular edema within the last 6 months

    Exclusion Criteria:
    • Blood glucose was not controlled steadily(HbA1cd≥10%)

    • Accompanied with severe hypertension(BP≥180/110mmHg)

    • Taking part in other clinical trial within 3 months

    • Planning panretinal photocoagulation(PRP) within 3 months

    • Performed cataract surgery in the last 3 months

    • Accompanied with other retinal vascular disease that can lead to macular edema, for example branch retinal vein occlusion(BRVO),central retinal vein occlusion(CRVO)

    • Accompanied with severe opacity of refractive media that maybe impact therapy and observation

    • Accompanied with nystagmus

    • Accompanied with some history that maybe interfere with result or increase the risk of patients

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Zhongshan Ophthalmic Center, Sun Yat-sen University Guangzhou Guangdong China 510060

    Sponsors and Collaborators

    • Sun Yat-sen University

    Investigators

    • Study Chair: Chenjin Jin, Ph.D, State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Jin Chen-jin, Professor,Dr, Sun Yat-sen University
    ClinicalTrials.gov Identifier:
    NCT03641144
    Other Study ID Numbers:
    • NLPD-ZOC
    First Posted:
    Aug 21, 2018
    Last Update Posted:
    Aug 21, 2018
    Last Verified:
    Aug 1, 2018
    Individual Participant Data (IPD) Sharing Statement:
    Undecided
    Plan to Share IPD:
    Undecided
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Jin Chen-jin, Professor,Dr, Sun Yat-sen University
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Aug 21, 2018