NCT Number: NCT01203540
Evaluation of the Effect and Tolerance of Preservative Free NAAGA on the Inflammatory Component and Symptoms of Dry Eye Syndrome in Allergic Conjunctivitis Patients
Multicentre, Double blind, Randomized, Comparative Study(comparing N-acetyl-aspartyl-glutamic acid(NAAGA) in Abak preservative free device versus SALINE in Abak preservative free device.
Evaluation of the effects and safety of NAABAK® through inflammation markers and symptoms in patients with allergic conjunctivitis and dry eye syndrome after 3 months treatment.
The patients will attend 4 visits.
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Notify MeKey information
Conditions
Age range
20 year and older
Sex eligibility
All sexes
Study type
Interventional
Phase
Phase 4
Primary location
Seoul National University Bundang Hospital, Seongnam-si, South Korea
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Age ≥ 20 years old
- Patients with dry eye syndrome in allergic conjunctivitis
Exclusion criteria
- Severe dry eye syndrome
- Severe ocular pathology
Treatment and study plan
Saline eyedrops
DrugSponsors and collaborators
Lead sponsor
Laboratoires Thea
Industry
Collaborators
- Samil Pharmaceutical Co., Ltd.
Registry information
Important dates
- Study start
- 2010
- Study completion
- 2011
- First posted
- Sep 16, 2010
- Registry last updated
- Jan 31, 2012
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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