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Comparative Study of 0.5% Carboxymethylcellulose With 0.005% Stabilized Oxychlorocomplex (PURITE™) Versus 0.5% Carboxymethylcellulose in the Treatment of Dry Eye

NCT00386646 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 100

Last updated 2015-06-03

No results posted yet for this study

Summary

To compare if 0.5% carboxymethylcellulose with 0.005% SOC (Stabilized oxychloro complex) have the same effectiveness and safety as 0.5% carboxymethylcellulose on dry eye patients.

Conditions

  • Dry Eye Syndromes

Interventions

DRUG

0.5% carboxymethylcellulose (CMC) with purite and CMC alone

Sponsors & Collaborators

  • Chulalongkorn University

    lead OTHER

Principal Investigators

  • Pitipong Suramethakul, MD · Faculty of Medicine, Chulalongkorn University, Bangkok Thailand

  • Vilavun Puangsricharern, MD · Faculty of Medicine, Chulalongkorn University, Bangkok Thailand

  • Nipaporn Maneerat, MD · Faculty of Medicine, Chulalongkorn University, Bangkok Thailand

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2004-02-29
Completion
2005-10-31

Countries

  • Thailand

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00386646 on ClinicalTrials.gov