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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT02524431
Other study ID # 14-430E
Secondary ID
Status Withdrawn
Phase N/A
First received August 6, 2015
Last updated November 18, 2016
Start date November 2014
Est. completion date January 2016

Study information

Verified date November 2016
Source Wills Eye
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

The purpose of this study is to try to identify the cause of damage to the drainage system of the eye (the trabecular meshwork). Damage to this system may cause elevation in the pressure within the eye and thereby damage to the optic nerve and the vision.


Description:

During a routine trabeculectomy surgery, a corneo-scleral block that includes TM tissue will be collected at the operating room. This tissue is routinely removed during every trabeculectomy surgery. The tissue will be stored immediately in normal saline at 4 degrees Celsius, and walked directly to the Jefferson Center for Translational Medicine at Thomas Jefferson University by the Wills eye glaucoma research fellow. TM tissue will be identified using light microscope base on TM cell pigmentation. The ocular tissue will be fixed and placed in pre-cooled fixative on ice for 1 hour. The lengths of mitochondrial cross sections at the longest extent will be measured under electron microscopy (EM) in order to identify the mitochondrial dynamics. Quantitative Polymerase Chain Reaction (qPCR) will be done to identify proteins responsible for mitochondrial fusion.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date January 2016
Est. primary completion date January 2016
Accepts healthy volunteers No
Gender Both
Age group 21 Years to 80 Years
Eligibility Inclusion Criteria:

- Minimum 2-year diagnosis of POAG

- Moderate to advanced stage of the disease

- DDLS stages 5 through 10 with visual field loss

- Age between 21 and 80 years

- Planned trabeculectomy with or without concomitant cataract surgery

Exclusion Criteria:

- Age = 20 years old

- Any other type of glaucoma other than POAG

- Patients who had undergone selective laser trabeculoplasty (SLT) or argon laser trabeculoplasty (ALT)

- Patients with history of ocular trauma

- Patients with previous eye surgery will be excluded both from the study and the control groups

Study Design

Allocation: Non-Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Basic Science


Related Conditions & MeSH terms


Intervention

Other:
Collection of trabecular meshwork tissue during surgery
Tissue is collected during surgery at Wills Eye and then processed at thomas jefferson to identify the trabecular meshwork using light microscope. The ocular tissue will be fixed and the mitochondrial cross sections at the longest extent will be measured under electron microscopy (EM) in order to identify the mitochondrial dynamics. Quantitative Polymerase Chain Reaction (qPCR) will be done to identify proteins responsible for mitochondrial fusion.

Locations

Country Name City State
United States Wills Eye Hospital Philadelphia Pennsylvania

Sponsors (2)

Lead Sponsor Collaborator
Wills Eye Thomas Jefferson University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary 3-D EM tomography for mitochondria obtained from sample tissue 1 year No
Secondary Gene expression of Drp1 1 year No
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