Comparing Effects of Two Fixed Combinations Ophthalmic Solutions on Ocular Blood Flow

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
Allergan
ClinicalTrials.gov Identifier:
NCT00811850
First received: December 17, 2008
Last updated: July 25, 2012
Last verified: July 2012

December 17, 2008
July 25, 2012
December 2008
December 2009   (final data collection date for primary outcome measure)
  • Retrobulbar Blood Flow (Peak Systolic Velocity) as Measured by Color Doppler Imaging in the Nasal Short Posterior Ciliary Artery [ Time Frame: 1 Month ] [ Designated as safety issue: No ]
    Peak systolic velocity (PSV) of retrobulbar blood flow as measured by color Doppler imaging (CDI) in the nasal short posterior ciliary artery after 1 month of treatment. CDI is a high-resolution ultrasound system which provides visualization of the flow of blood through a vessel. PSV is the maximum blood flow speed within a vessel at the time of systole (maximum pressure exerted in a blood vessel).
  • Retrobulbar Blood Flow (End Diastolic Velocity) as Measured by Color Doppler Imaging in the Nasal Short Posterior Ciliary Artery [ Time Frame: 1 Month ] [ Designated as safety issue: No ]
    End diastolic velocity (EDV) of retrobulbar blood flow as measured by color Doppler imaging (CDI) in the nasal short posterior ciliary artery after 1 month of treatment. CDI is a high-resolution ultrasound system which provides visualization of the flow of blood through a vessel. EDV is the maximum blood flow speed within a vessel at the end of diastole (minimum pressure exerted in a blood vessel in between heart beats).
  • Retrobulbar Blood Flow (Peak Systolic Velocity) as Measured by Color Doppler Imaging in the Temporal Short Posterior Ciliary Artery [ Time Frame: 1 Month ] [ Designated as safety issue: No ]
    Peak systolic velocity (PSV) of retrobulbar blood as measured by color Doppler imaging (CDI) in the temporal short posterior ciliary artery after 1 month of treatment. CDI is a high-resolution ultrasound system which provides visualization of the flow of blood through a vessel. PSV is the maximum blood flow speed within a vessel at the time of systole (maximum pressure exerted in the blood vessel).
  • Retrobulbar Blood Flow (End Diastolic Velocity) as Measured by Color Doppler Imaging in the Temporal Short Posterior Ciliary Artery [ Time Frame: 1 Month ] [ Designated as safety issue: No ]
    End diastolic velocity (EDV) of retrobulbar blood flow as measured by color Doppler imaging (CDI) in the temporal short posterior ciliary artery after 1 month of treatment. CDI is a high-resolution ultrasound system which provides visualization of the flow of blood through a vessel. EDV is the maximum blood flow speed within a vessel at the end of diastole (minimum pressure exerted in a blood vessel in between heart beats).
  • Retrobulbar Blood Flow (Peak Systolic Velocity) as Measured by Color Doppler Imaging in the Ophthalmic Artery [ Time Frame: 1 Month ] [ Designated as safety issue: No ]
    Peak systolic velocity (PSV) of retrobulbar blood flow as measured by color Doppler imaging (CDI) in the ophthalmic artery after 1 month of treatment. CDI is a high-resolution ultrasound system which provides visualization of the flow of blood through a vessel. PSV is the maximum blood flow speed within a vessel at the time of systole (maximum pressure exerted in a blood vessel).
  • Retrobulbar Blood Flow (End Diastolic Velocity) as Measured by Color Doppler Imaging in the Ophthalmic Artery [ Time Frame: 1 Month ] [ Designated as safety issue: No ]
    End diastolic velocity (EDV) of retrobulbar blood flow as measured by color Doppler imaging (CDI) in the ophthalmic artery after 1 month of treatment. CDI is a high-resolution ultrasound system which provides visualization of the flow through a vessel. EDV is the maximum blood flow speed within a vessel at the end of diastole (minimum pressure exerted in a blood vessel in between heart beats).
  • Retrobulbar Blood Flow (Peak Systolic Velocity) as Measured by Color Doppler Imaging in the Central Retinal Artery [ Time Frame: 1 Month ] [ Designated as safety issue: No ]
    Peak systolic velocity (PSV) of retrobulbar blood flow as measured by color Doppler imaging (CDI) in the central retinal artery after 1 month of treatment. CDI is a high-resolution ultrasound system which provides visualization of the flow of blood through a vessel. PSV is the maximum blood flow speed within a vessel at the time of systole (maximum pressure exerted in a blood vessel).
  • Retrobulbar Blood Flow (End Diastolic Velocity) as Measured by Color Doppler Imaging in the Central Retinal Artery [ Time Frame: 1 Month ] [ Designated as safety issue: No ]
    End diastolic velocity (EDV) of retrobulbar blood flow as measured by color Doppler imaging (CDI) in the central retinal artery after 1 month of treatment. CDI is a high-resolution ultrasound system which provides visualization of the flow of blood through a vessel. EDV is the maximum blood flow speed within a vessel at the end of diastole (minimum pressure exerted in a blood vessel in between heart beats).
retrobulbar blood flow [ Time Frame: Week 5 and Week 10 ] [ Designated as safety issue: No ]
Complete list of historical versions of study NCT00811850 on ClinicalTrials.gov Archive Site
Not Provided
Adverse Events [ Time Frame: Week 5 and Week 10 ] [ Designated as safety issue: No ]
Not Provided
Not Provided
 
Comparing Effects of Two Fixed Combinations Ophthalmic Solutions on Ocular Blood Flow
Not Provided

A 10 week evaluation, crossover design study including a 3 week washout period between treatments, to determine the effects of Combigan® (fixed combination brimonidine tartrate 0.2%/timolol maleate 0.5%) and Cosopt® (fixed combination dorzolamide hydrochloride-timolol maleate ophthalmic solutions) on ocular blood flow as measured by retrobulbar blood flow.

Not Provided
Interventional
Phase 4
Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Crossover Assignment
Masking: Double Blind (Investigator, Outcomes Assessor)
Primary Purpose: Treatment
Glaucoma
  • Drug: fixed combination of brimonidine tartrate 0.2% timolol maleate 0.5% ophthalmic solution
    1 drop of study medication taken approximately 12 hours apart, dosed 2 times a day for a total of two weeks
    Other Name: Combigan®
  • Drug: fixed combination of dorzolamide hydrochloride timolol maleate ophthalmic solution
    1 drop of study medication taken approximately 12 hours apart, dosed 2 times a day for a total of two weeks
    Other Name: Cosopt®
  • Active Comparator: Combigan®
    Combigan® (fixed combination of brimonidine tartrate 0.2%/timolol maleate 0.5% ophthalmic solution). One drop of study medication taken approximately 12 hours apart, dosed 2 times a day for a total of two weeks.
    Intervention: Drug: fixed combination of brimonidine tartrate 0.2% timolol maleate 0.5% ophthalmic solution
  • Active Comparator: Cosopt®
    Cosopt® (fixed combination of dorzolamide hydrochloride - timolol maleate ophthalmic solution). One drop of study medication taken approximately 12 hours apart, dosed 2 times a day for a total of two weeks.
    Intervention: Drug: fixed combination of dorzolamide hydrochloride timolol maleate ophthalmic solution
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
15
December 2009
December 2009   (final data collection date for primary outcome measure)

Inclusion Criteria:

  1. Age: 30 years or older.
  2. Primary open-angle glaucoma (POAG) or ocular hypertensive in at least one eye.
  3. Best corrected visual acuity at least 20/40 in at least one eye.

Exclusion Criteria:

  1. History of acute angle-closure or a narrow, occludable anterior chamber angle by gonioscopy.
  2. History of chronic or recurrent inflammatory eye diseases (e.g., scleritis, uveitis).
  3. History or signs of intraocular trauma.
  4. Any abnormality preventing reliable applanation tonometry.
  5. Current use of any ophthalmic or systemic steroid which may interfere with this investigation.
  6. Severe, unstable or uncontrolled cardiovascular, renal, or pulmonary disease.
Both
30 Years and older
No
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT00811850
GMA-COM-08-009
No
Allergan
Allergan
Not Provided
Study Director: Medical Director Allergan
Allergan
July 2012

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP