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Pars Plana Surgical Capsulotomy for Posterior Capsular Opacification (Capsulotomy)

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00964613
First Posted: August 25, 2009
Last Update Posted: August 7, 2015
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Collaborator:
Pakistan Ministry of Health
Information provided by (Responsible Party):
Jamshed Ahmed, Dow University of Health Sciences
  Purpose
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.

Condition
Blindness

Study Type: Observational
Study Design: Observational Model: Case-Only
Time Perspective: Prospective
Official Title: Pars Plana Surgical Capsulotomy for Posterior Capsular Opacification

Further study details as provided by Jamshed Ahmed, Dow University of Health Sciences:

Enrollment: 176
Study Start Date: January 2008
Study Completion Date: January 2009
Primary Completion Date: January 2009 (Final data collection date for primary outcome measure)
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
  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   1 Year to 95 Years   (Child, Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
Patients having posterior capsular opacification
Criteria

Inclusion Criteria:

  • Patients with Posterior capsular opacification
  • Both Sexes
  • All ages

Exclusion Criteria:

  • Retinal disease
  • Uncontrolled Glaucoma
  • Corneal opacity
  Contacts and Locations
No Contacts or Locations Provided
  More Information

Responsible Party: Jamshed Ahmed, Assistant Professor, Dow University of Health Sciences
ClinicalTrials.gov Identifier: NCT00964613     History of Changes
Other Study ID Numbers: Surgical Capsulotomy
First Submitted: August 24, 2009
First Posted: August 25, 2009
Last Update Posted: August 7, 2015
Last Verified: August 2015

Keywords provided by Jamshed Ahmed, Dow University of Health Sciences:
Pars Plana
Surgical Capsulotomy
Posterior capsule opacification
visual outcome
Complications

Additional relevant MeSH terms:
Blindness
Vision Disorders
Sensation Disorders
Neurologic Manifestations
Nervous System Diseases
Eye Diseases
Signs and Symptoms