A Clinical Trial of Phacoemulsification Versus Phacoemulsification & the iStent Implantation in POAG Patients
Primary Purpose
Primary Open Angle Glaucoma and Cataracts
Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
phacoemulsification alone
iStent Trabecular Micro-Bypass Stent
Sponsored by
About this trial
This is an interventional treatment trial for Primary Open Angle Glaucoma and Cataracts focused on measuring POAG, Combination glaucoma & cataract procedure, trabecular micro-bypass stent, iStent
Eligibility Criteria
Inclusion Criteria:
- a previous diagnosis of POAG
- an IOP of > 18 mm Hg at three separate visits if on one medication, or subjects on at least two medications with uncontrolled IOP on three separate visits.
- all patients were deemed likely to follow surgeon instructions and were able to give informed consent.
Exclusion Criteria:
- any glaucoma diagnosis other than POAG
- the presence of peripheral anterior synechiae (PAS)
- a cloudy cornea likely to inhibit gonioscopic view of the angle
- any previous ocular surgery
- history of trauma or ocular surface disease
- the presence of peripheral anterior synechiae (PAS)
- a cloudy cornea likely to inhibit gonioscopic view of the angle
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
1
2
Arm Description
phacoemulsification alone
phacoemulsification and implantation of the iStent® trabecular micro-bypass stent
Outcomes
Primary Outcome Measures
Primary outcomes included IOP and reduction in medication use.
Secondary Outcome Measures
Full Information
NCT ID
NCT00847158
First Posted
February 18, 2009
Last Updated
February 18, 2009
Sponsor
University of Turin, Italy
1. Study Identification
Unique Protocol Identification Number
NCT00847158
Brief Title
A Clinical Trial of Phacoemulsification Versus Phacoemulsification & the iStent Implantation in POAG Patients
Official Title
A Randomized, Double-Masked Clinical Trial of Phacoemulsification Compared With Phacoemulsification and Micro-Bypass Stent Implantation in Patients With POAG
Study Type
Interventional
2. Study Status
Record Verification Date
February 2009
Overall Recruitment Status
Completed
Study Start Date
December 2006 (undefined)
Primary Completion Date
March 2008 (Actual)
Study Completion Date
March 2008 (Actual)
3. Sponsor/Collaborators
Name of the Sponsor
University of Turin, Italy
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
This was a prospective, double-masked, 15-month clinical trial comparing efficacy of phacoemulsification alone to combined phacoemulsification and implantation of the iStent® trabecular micro-bypass stent in patients with primary open-angle glaucoma.
Detailed Description
This was a prospective, randomized open-label study of 36 patients with POAG scheduled to undergo phacoemulsification with intraocular lens implantation ("cataract surgery"). Patients were randomized 2:1 to receive either cataract surgery alone (control group) or cataract surgery and iStent implantation (combined surgery group).
Implantation of the study stent occurred after cataract extraction and IOL insertion using the same small, temporal, clear-corneal incision (approximately 3 mm) used to perform phacoemulsification and IOL placement. The study stent was guided into Schlemm's canal using ab-interno gonioscopy (using a Swan-Jacobs gonioscope). (Figure 1) If no complications occurred during phacoemulsification, acetylcholine was injected in the anterior chamber after the IOL implantation to constrict the pupil. The anterior chamber was then filled with a viscoelastic agent to reform the anterior chamber and provide more clearance in the angle.
The anterior chamber was traversed with the applicator (the implant was on the tip of applicator) and the trabecular meshwork located. The leading edge of the device was gently slid through the trabecular meshwork and into Schlemm's canal at the nasal position (3 to 4 o'clock for the right eye; 9 to 8 o'clock for the left eye) with the tip of the implant directed inferiorly. If difficulty was encountered with the insertion at the primary location, we tried inserting about 0.5 clock hour inferiorly; and continued to move inferiorly as needed for subsequent attempts. Next, the device was released by pushing the button on the applicator, position of the stent was verified and the applicator was withdrawn.
The patients were instructed to discontinue all glaucoma medications after surgery. Standard post cataract extraction antibiotic and anti-inflammatory drug regimen was prescribed. Target pressure for each patient was determined prior to study entry. Following the assigned procedure, any patient with an IOP (as measured between 8 and 10 AM) that was greater than 2 mm Hg over their target was instructed to return twice in the following three days for re-measurement of their IOP. If the patient's IOP was > 2 mm Hg over their target pressure, ocular hypotensive agents were added. The medications were added in a pre-set schedule, with beta-blockers first, angiotensin-converting enzyme (ACE) inhibitors second, and prostaglandins third. If, however, on the third consecutive visit the patient's IOP was within 2 mm Hg of target, patient re-entered the normal visit schedule. Investigators were masked to treatment assignment both when measuring IOP and when determining when or if to add medications.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Primary Open Angle Glaucoma and Cataracts
Keywords
POAG, Combination glaucoma & cataract procedure, trabecular micro-bypass stent, iStent
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
36 (Actual)
8. Arms, Groups, and Interventions
Arm Title
1
Arm Type
Active Comparator
Arm Description
phacoemulsification alone
Arm Title
2
Arm Type
Active Comparator
Arm Description
phacoemulsification and implantation of the iStent® trabecular micro-bypass stent
Intervention Type
Procedure
Intervention Name(s)
phacoemulsification alone
Other Intervention Name(s)
cataract surgery, Phaco
Intervention Description
phacoemulsification alone
Intervention Type
Device
Intervention Name(s)
iStent Trabecular Micro-Bypass Stent
Other Intervention Name(s)
iStent, Trabecular micro-bypass stent, GTS100L, GTS100R
Intervention Description
phacoemulsification and implantation of the iStent® trabecular micro-bypass stent
Primary Outcome Measure Information:
Title
Primary outcomes included IOP and reduction in medication use.
Time Frame
15 month
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
a previous diagnosis of POAG
an IOP of > 18 mm Hg at three separate visits if on one medication, or subjects on at least two medications with uncontrolled IOP on three separate visits.
all patients were deemed likely to follow surgeon instructions and were able to give informed consent.
Exclusion Criteria:
any glaucoma diagnosis other than POAG
the presence of peripheral anterior synechiae (PAS)
a cloudy cornea likely to inhibit gonioscopic view of the angle
any previous ocular surgery
history of trauma or ocular surface disease
the presence of peripheral anterior synechiae (PAS)
a cloudy cornea likely to inhibit gonioscopic view of the angle
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Antonio Fea, MD
Organizational Affiliation
University of Torino
Official's Role
Principal Investigator
12. IPD Sharing Statement
Citations:
PubMed Identifier
26587282
Citation
Fea AM, Consolandi G, Zola M, Pignata G, Cannizzo P, Lavia C, Rolle T, Grignolo FM. Micro-Bypass Implantation for Primary Open-Angle Glaucoma Combined with Phacoemulsification: 4-Year Follow-Up. J Ophthalmol. 2015;2015:795357. doi: 10.1155/2015/795357. Epub 2015 Oct 26.
Results Reference
derived
Learn more about this trial
A Clinical Trial of Phacoemulsification Versus Phacoemulsification & the iStent Implantation in POAG Patients
We'll reach out to this number within 24 hrs