- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00964613
Pars Plana Surgical Capsulotomy for Posterior Capsular Opacification (Capsulotomy)
August 6, 2015 updated by: Jamshed Ahmed, Dow University of Health Sciences
Cataract is a leading cause of Global blindness.
After cataract surgery nearly half of the people become blind due to posterior capsular opacification.
The only solution for this problem is LASER capsulotomy.
Laser machine is not available in remote areas especially in underdeveloped countries.
The solution of this problem is surgical capsulotomy which can be performed any where.
Study Overview
Status
Completed
Conditions
Detailed Description
posterior capsular opacification is treated by YAG laser capsulotomy.
this require sophisticated technology ans specific environment which is not possible in underdeveloped countries.
we describe a method in which posterior capsular opacification could be managed by using only a 27 Gauge needle through pars plana.
opacified posterior capsule is under tension that is why a small puncture results in a large central opening
Study Type
Observational
Enrollment (Actual)
176
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
1 year to 95 years (Child, Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Patients having posterior capsular opacification
Description
Inclusion Criteria:
- Patients with Posterior capsular opacification
- Both Sexes
- All ages
Exclusion Criteria:
- Retinal disease
- Uncontrolled Glaucoma
- Corneal opacity
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Collaborators
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
January 1, 2008
Primary Completion (Actual)
January 1, 2009
Study Completion (Actual)
January 1, 2009
Study Registration Dates
First Submitted
August 24, 2009
First Submitted That Met QC Criteria
August 24, 2009
First Posted (Estimate)
August 25, 2009
Study Record Updates
Last Update Posted (Estimate)
August 7, 2015
Last Update Submitted That Met QC Criteria
August 6, 2015
Last Verified
August 1, 2015
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- Surgical Capsulotomy
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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