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Comparison Between Bandage Contact Lens and Pressure Patching for The Erosion Area and Pain Scale in Corneal Erosion Patients

Comparison Between Bandage Contact Lens and Pressure Patching for The Erosion Area and Pain Scale in Corneal Erosion Patients

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01809483
Enrollment
32
Registered
2013-03-12
Start date
2012-09-30
Completion date
2013-02-28
Last updated
2013-03-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Erosion; Cornea, Traumatic

Keywords

mechanical corneal erosion, bandage contact lens, pressure patching, erosion area, pain scale

Brief summary

This research aims to compare between bandage contact lens and pressure patching in reducing size of erosion area and pain scale in corneal erosion patients as well as its complications.

Detailed description

This is a randomized open-label clinical trial in patients with mechanical corneal erosion. Subjects were selected to use bandage contact lens (Senofilcon A) or pressure patching. All subjects received combination of Polymyxin B, Neomycin, and Gramicidin eye drops and 0,5% Tropicamide eye drops. Evaluation was done 24 hours after treatment

Interventions

Bandage contact lens : contact lenses (material senofilcon A; base curve 8,8 mm; power - 0,50; diameter 14 mm)

DEVICEPressure patching

Pressure patching : using 2 pieces of sterile gauze. The first gauze placed vertically and the second placed horizontally, then fixed with adhesive tape so that eyelid can not move.

Sponsors

Udayana University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
17 Years to 55 Years
Healthy volunteers
No

Inclusion criteria

* aged 17-55 years * onset of corneal erosion \< 48 hours * corneal erosion due to mechanical injury * extensive corneal erosion \> 3 mm2

Exclusion criteria

* bilateral corneal erosion * corneal erosion due to chemical or thermal injury * history of systemic analgesic use within 1 week prior to the examination or topical analgesics within 1 hour before the examination * history of systemic or topical antibiotics within 1 week prior to the examination * other abnormalities due to trauma * palpebral or eyelashes position abnormalities * anterior segment infections * tear break-up time \< 7 seconds in the contra lateral eye

Design outcomes

Primary

MeasureTime frameDescription
Size of corneal erosion area24 hourCorneal erosion area is the multiplication of the long and short axis of corneal erosion, as measured using a caliper, with the help of fluorescein and cobalt blue slit lamp beam

Secondary

MeasureTime frameDescription
Pain scale24 hourPain scale assessment conducted using the Visual Analogue Scale (VAS) subjectively

Other

MeasureTime frameDescription
Complication24 hourComplication of corneal erosion (e.g. conjunctivitis, keratitis, corneal ulcer)

Countries

Indonesia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026