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Preferred treatment for removal of corneal rust

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN22641495
Enrollment
Unknown
Registered
2005-09-30
Start date
2003-02-27
Completion date
Unknown
Last updated
2015-01-13

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

Conditions

Eye Diseases: Corneal damage Eye Diseases Corneal damage

Interventions

Patients will be randomly allocated 2 or 5 days using sealed envelopes. The following will be undertaken: 1.Case History, 2.Visual Acuity, 3. Examination: Slit lamp bio microscopy 4. Check whether p

Sponsors

Record Provided by the NHSTCT Register - 2005 Update - Department of Health (UK)
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Not provided at time of registration

Exclusion criteria

Exclusion criteria: Not provided at time of registration

Design outcomes

Primary

MeasureTime frame
Aims & Objectives: To identify what is the best practice for removal of cornea rust, ensuring that patient care is not compromised. To compare differences in discomfort felt by the patient and healing process of the cornea when visits are at 2 or 5 day intervals. Study endpoints: To compare ease and completion of removal of cornea rust.—

Secondary

MeasureTime frame
Not provided at time of registration—

Countries

United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026