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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01125540
Other study ID # Allergy02
Secondary ID
Status Completed
Phase N/A
First received May 17, 2010
Last updated May 17, 2010
Start date June 2007
Est. completion date January 2010

Study information

Verified date May 2010
Source Aston University
Contact n/a
Is FDA regulated No
Health authority United Kingdom: Research Ethics Committee
Study type Interventional

Clinical Trial Summary

Patients with seasonal allergic conjunctivitis are normally advised to avoid contact lens wear when they are having symptoms. However, modern soft contact lenses which are disposed of daily offer the potential to protect and lubricate the ocular surface. This study examines this possible effect.


Recruitment information / eligibility

Status Completed
Enrollment 10
Est. completion date January 2010
Est. primary completion date January 2010
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- contact lens wearer

- proven allergy to grass pollen

Exclusion Criteria:

- eye disease

- ocular medication

- allergy medication

- asthma

Study Design

Allocation: Randomized, Intervention Model: Single Group Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Prevention


Related Conditions & MeSH terms


Intervention

Device:
Acuvue (Standard Daily Disposable Contact Lens)

CIBA Dailies Aquacomfort Plus (Contact Lens - enhance lubricating)


Locations

Country Name City State
United Kingdom Aston University Birmingham West Midlands

Sponsors (2)

Lead Sponsor Collaborator
Aston University National Pollen and Aerobiology Unit, Worcester

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Symptoms Subjective rating of itchyness, dryness, burning, watering and discomfort 4 hours No
Primary Signs Signs of bulbar, limbal and palpebtal hyperaemia and staining 4 hours No