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Active, Not Recruiting

NCT Number: NCT01969786

Village Integrated Eye Workers Trial

VIEW is a community-randomized trial designed to determine whether it is possible to prevent corneal ulcers on a large scale. The study compares the incidence of corneal ulceration between villages in which volunteers are trained to diagnose and treat corneal abrasions and villages which receive no intervention.

Active, Not Recruiting

This study is active but is not currently recruiting participants.

Key information

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Bharatpur Eye Hospital - Seva Foundation

Bharatpur, Nepal

About this study

Corneal ulceration is a leading cause of visual impairment globally, with a disproportionate burden in developing countries. Corneal opacity after ulceration is responsible for a significant proportion of blinding eye disease in Africa and Asia. While antimicrobial treatment is generally effective in eradicating infection, "successful" treatment is often associated with a poor visual outcome. The scarring that accompanies the resolution of infection leaves many eyes blind. It has been difficult to discern differences between different antimicrobials in a randomized controlled trial (RCT). In fact, only a single RCT with more than 50 subjects has found any significant difference between ulcer treatments. Thus, prevention of corneal ulceration may be our best opportunity to reduce morbidity associated with corneal ulceration.

Several non-randomized prevention studies in Nepal, Myanmar, and Bhutan have suggested that antibiotic ointment applied promptly after a corneal abrasion could dramatically lower the incidence of ulcers, relative to neighboring or historic controls. In Madurai, South India, a clinical trial demonstrated that abrasions randomized to topical antibacterial and antifungal prophylaxis were not significantly less likely to develop fungal ulcers than those randomized to antibacterial ointment alone, even though the region had a high incidence of fungal infection. This same trial also found that the incidence of ulcers in villages outside the prophylaxis program was far higher; these control villages were neighboring but not randomized, and it is possible that they were in some way different from the villages included in the program.

VIEW was designed to determine whether we can prevent corneal ulcers on a large scale. VIEW is a community-randomized trial comparing villages randomized to receive an intervention consisting of a trained community health volunteer providing antimicrobial ointment after a corneal abrasion to control villages receiving no additional intervention. The primary outcome of corneal ulcer will be measured by baseline and annual population-based census performed in both intervention and control villages by masked examiners from baseline to 36 months. The examiners will photograph corneas of all residents who are suspected of having a corneal ulcer, with photographs later read by masked examiners. Each resident in the village will be examined for evidence of a corneal opacity and asked about their ocular history. In villages randomized to intervention, the trained community health volunteers will actively promote their services through regular meetings with local women's groups by encouraging residents to notify the village eye health worker within 24 hours of ocular trauma. In control villages, abrasions and ulcers will be treated if they present to a clinic or are found during the annual monitoring visits, but active promotion of corneal abrasion care will not be offered.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Presence of a corneal abrasion
  • Willingness to be treated with topical antibiotic and antifungal ointments 3 times a day for 3 days
  • Appropriate consent

Exclusion criteria

  • Evidence of a corneal ulcer
  • Evidence of other acute eye disease requiring urgent care
  • Known allergy to study medications
  • Not willing to participate

Treatment and study plan

Corneal ulcer prevention program

Other

The corneal ulcer prevention intervention consists of training female community health volunteers to diagnose corneal abrasions and to treat the abrasions with 1% itraconazole and 1% chloramphenicol ointments 3 times a day for 3 days.

Primary outcomes

  1. Incidence of corneal ulceration in the two study arms as measured by corneal photography

    Time frame: 3 years

Secondary outcomes

  1. Trial-based cost effectiveness analysis to determine the incremental cost per corneal ulcer prevented

    Time frame: 3 years

Other outcomes

  1. Incidence of corneal ulceration in the non-intervention arm corrected by passive surveillance

    Time frame: 3 years

  2. Long-term follow-up of incidence of corneal ulceration in the two study arms as measured by corneal photography

    Time frame: 5 years

Sponsors and collaborators

Lead sponsor

University of California, San Francisco

Other

Collaborators

  • Bharatpur Eye Hospital
  • National Eye Institute (NEI)
  • Seva Foundation

Registry information

Acronym: VIEW

Important dates

Study start
2014
Primary completion
2026
Study completion
2026
First posted
Oct 25, 2013
Registry last updated
Apr 7, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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