Primary Open Angle GlaucomaNCT00327405
Results of Ocular Compression and Suture Release in Trabeculectomy and Combined Surgery
An observational study of Primary Open Angle Glaucoma, run by University of Cincinnati at 1 site in United States.
Trial summary
The use of ocular compression and suture release have helped to improve the safety and decrease the risks of glaucoma filtering surgery. This study looks at the decrease in intraocular pressure and glaucoma medications required following glaucoma filtering surgery. Read more about this study
- Who is it for?
- Ages 0 years and older
- Conditions the study is for
- Primary Open Angle Glaucoma
- How many people
- Not given
- Where
- 1 siteUnited States
- Study dates
- Start not givento not given
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 0 years and older
- All sexes
- No healthy volunteers
- Child, Adult, Older adult
Who may be able to join
- Primary Open Angle Glaucoma
- Six Months Followup
- No previous surgery
Who cannot join
- Less Than Six Months Followup
- Previous glaucoma surgery
Trial locations and contacts
1 site in 1 country.
About this study
Official title: A Retrospective Study of Surgical Outcomes.
The use of ocular compression and suture release have helped to improve the safety and decrease the risks of glaucoma filtering surgery. This study looks at the decrease in intraocular pressure and glaucoma medications required following glaucoma filtering surgery.
Read the detailed description
A retrospective review of surgical results in eyes with at least six months followup was performed for trabeculectomy and combined phacoemulsification-trabeculectomy surgery. A total of 141 eyes were studied.
- Conditions
- Primary Open Angle Glaucoma
- Keywords
- POAG, Primary Open Angle Glaucoma, Trabeculectomy, Combined Phacotrabeculectomy, Combined Glaucoma Cataract Surgery, Releasable Suture, Ocular Compresssion
- Medical subject headings
- Glaucoma, Open-Angle
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted18 May 2006 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Primary Open Angle GlaucomaStudies of the same condition, open and under way.
- More trials run by University of CincinnatiThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
Sponsor and investigators
- Lead sponsor
- University of Cincinnati
- Sponsor type
- University, hospital or other
- Investigators
- John S Cohen, MD, Principal investigator, University of Cincinnati Department of Ophthalmology
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT00327405
- Sponsor's protocol ID
- UCJSC001
- Status last verified
- Jan 2006
- First submitted
- 17 May 2006
- Last updated
- 18 May 2006
- Results posted
- No
Study at a glance
From the registry record, last updated by the sponsor on 18 May 2006. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Retrospective Study of Surgical Outcomes.
- ClinicalTrials.gov ID
- NCT00327405
- Acronym / sponsor ID
- UCJSC001
- Conditions
- Primary Open Angle Glaucoma
- Keywords
- POAG, Primary Open Angle Glaucoma, Trabeculectomy, Combined Phacotrabeculectomy, Combined Glaucoma Cataract Surgery, Releasable Suture, Ocular Compresssion
- Study type
- Observational
- Recruitment status
- Completed
- Lead sponsor
- University of CincinnatiUniversity, hospital or other
- First posted
- 18 May 2006 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The use of ocular compression and suture release have helped to improve the safety and decrease the risks of glaucoma filtering surgery. This study looks at the decrease in intraocular pressure and glaucoma medications required following glaucoma filtering surgery.
Detailed description
A retrospective review of surgical results in eyes with at least six months followup was performed for trabeculectomy and combined phacoemulsification-trabeculectomy surgery. A total of 141 eyes were studied.
Study design
Who may qualify
- Ages
- 0 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child, Adult, Older adult
Key inclusion criteria (3 listed)
- Primary Open Angle Glaucoma
- Six Months Followup
- No previous surgery
Key exclusion criteria (2 listed)
- Less Than Six Months Followup
- Previous glaucoma surgery
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
Not reported in the source record.
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 18 May 2006.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
John S Cohen, MD principal investigator
University of Cincinnati Department of Ophthalmology
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Primary Open Angle Glaucoma, run by University of Cincinnati at 1 site in United States.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 3 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 18 May 2006. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 18 May 2006.