A 6-Week Safety and Efficacy Study of Travatan Compared to Xalcom in Subjects With Open-Angle Glaucoma(OAG) or Ocular Hypertension(OHT)
This study has been completed.
Sponsor:
Alcon Research
Information provided by:
Alcon Research
ClinicalTrials.gov Identifier:
NCT00051155
First received: January 3, 2003
Last updated: August 4, 2008
Last verified: August 2008
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Purpose
To compare the safety and IOP-lowering efficacy of TRAVATAN and XALCOM in subjects with open-angle glaucoma or ocular hypertension.
| Condition | Intervention | Phase |
|---|---|---|
|
Glaucoma, Open-Angle Ocular Hypertension |
Drug: Travoprost (0.004%) Drug: Latanoprost (0.005%)/Timolol (0.5%) |
Phase 3 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Safety/Efficacy Study Intervention Model: Parallel Assignment Masking: Double-Blind Primary Purpose: Treatment |
| Official Title: | A 6-Week Safety and Efficacy Study of TRAVATAN Compared to XALCOM in Subjects With Open-Angle Glaucoma or Ocular Hypertension. |
Resource links provided by NLM:
Further study details as provided by Alcon Research:
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Criteria
Patients of any race and either sex with open-angle glaucoma (with or without pigment dispersion or pseudoexfoliation component) or ocular hypertension.
Contacts and Locations
More Information
No publications provided
| ClinicalTrials.gov Identifier: | NCT00051155 History of Changes |
| Other Study ID Numbers: | C-01-74 |
| Study First Received: | January 3, 2003 |
| Last Updated: | August 4, 2008 |
| Health Authority: | United States: Food and Drug Administration |
Keywords provided by Alcon Research:
|
Glaucoma POAG OAG OHT |
Additional relevant MeSH terms:
|
Glaucoma Glaucoma, Open-Angle Hypertension Ocular Hypertension Eye Diseases Vascular Diseases Cardiovascular Diseases |
Latanoprost Travoprost Antihypertensive Agents Cardiovascular Agents Therapeutic Uses Pharmacologic Actions |
ClinicalTrials.gov processed this record on May 23, 2013