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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01203540
Other study ID # NBKE_SNUBH&BM_01
Secondary ID LT0455-IST-01/10
Status Completed
Phase Phase 4
First received September 15, 2010
Last updated January 27, 2012
Start date October 2010
Est. completion date January 2011

Study information

Verified date January 2012
Source Laboratoires Thea
Contact n/a
Is FDA regulated No
Health authority Korea: Institutional Review Board
Study type Interventional

Clinical Trial Summary

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.


Recruitment information / eligibility

Status Completed
Enrollment 21
Est. completion date January 2011
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 20 Years and older
Eligibility Inclusion Criteria:

- Age = 20 years old

- Patients with dry eye syndrome in allergic conjunctivitis

Exclusion Criteria:

- Severe dry eye syndrome

- Severe ocular pathology

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Double-Blind, Primary Purpose: Treatment


Intervention

Drug:
NAABAK eyedrops

Saline eyedrops


Locations

Country Name City State
Korea, Republic of Seoul National University Bundang Hospital Seongnam-si
Korea, Republic of Seoul National University Boramae Medical Center Seoul

Sponsors (2)

Lead Sponsor Collaborator
Laboratoires Thea Samil Pharmaceutical Co., Ltd.

Country where clinical trial is conducted

Korea, Republic of, 

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