Sequential Laser Iridotomy Using Argon and Q-Switched 532 nm Frequency Doubled Neodymium Yag Laser: A Pilot Study
1 other identifier
interventional
10
1 country
1
Brief Summary
Sequential Laser Iridotomy uses argon and Nd:yag laser in the first and second steps, respectively. Using q-switched 532 nm laser in the second step is hypothesized to be as good and effective as the conventional Nd:yag laser, because it selectively targets pigmented cells and delivers a short pulse duration of 3 nanoseconds, causing less thermal and collateral damage.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Nov 2006
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
November 1, 2006
CompletedFirst Submitted
Initial submission to the registry
March 27, 2007
CompletedFirst Posted
Study publicly available on registry
March 28, 2007
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2007
CompletedStudy Completion
Last participant's last visit for all outcomes
December 1, 2007
CompletedMay 14, 2008
May 1, 2008
1.1 years
March 27, 2007
May 12, 2008
Conditions
Keywords
Outcome Measures
Primary Outcomes (9)
Visual Acuity
Intraocular pressure
Total power delivered by each laser modality
Iridotomy patency and size
Pain rating during the procedure
Anterior segment inflammation
Endothelial cell count
Cataract progression
Rate of complications
Interventions
Eligibility Criteria
You may qualify if:
- More than 21 years old
- Able to give informed consent
- Diagnosis of either: chronic angle closure glaucoma (CACG), primary angle closure (PAC), primary angle closure suspect (PACS) or fellow eyes of acute angle closure glaucoma (AACG), and in need of a laser iridotomy
You may not qualify if:
- History of any prior laser treatment or intraocular surgery to the eye
- History of any corneal disease
- Any ocular infection/ inflammation within the last two months
- Inability to give informed consent
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
National University Hospital
Singapore, 119074, Singapore
Related Publications (1)
Latina MA, Park C. Selective targeting of trabecular meshwork cells: in vitro studies of pulsed and CW laser interactions. Exp Eye Res. 1995 Apr;60(4):359-71. doi: 10.1016/s0014-4835(05)80093-4.
PMID: 7789416BACKGROUND
Study Officials
- PRINCIPAL INVESTIGATOR
Paul Chew, FRCSEd,MMed
National University Hospital, Singapore
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NON RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
Study Record Dates
First Submitted
March 27, 2007
First Posted
March 28, 2007
Study Start
November 1, 2006
Primary Completion
December 1, 2007
Study Completion
December 1, 2007
Last Updated
May 14, 2008
Record last verified: 2008-05