Anti-Aggregative Therapy and Laser Iridectomy

NCT ID: NCT00426400

Last Updated: 2007-01-24

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

PHASE4

Study Classification

INTERVENTIONAL

Study Start Date

2006-03-31

Brief Summary

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Our study investigates the effect of anti-aggregative treatment on success and complications of laser iridectomy. The study includes patients scheduled for laser iridectomy due to narrow angles.Patients will undergo first laser treatment with the anti-aggregative treatment and will scheduled for next lase in the other eye after discontinuing the anti-aggregative treatment. The patients will be followed-up for 3 months.

Detailed Description

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Conditions

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Eyes With Narrow Angle

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Interventions

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The cessation of anti-aggregative treatment for 10 days

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* patients with narrow angle that need laser iridectomy and take anti- aggregative treatment
* over 20 years old
* patients who can stop their anti-aggregative treatment for 10 days

Exclusion Criteria

* under coumadin treatment
* post ocular surgeries
Minimum Eligible Age

20 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Sheba Medical Center

OTHER_GOV

Sponsor Role lead

Principal Investigators

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Hani Levkovitch-Verbin, MD

Role: PRINCIPAL_INVESTIGATOR

Goldscheleger Eye Institute, Sheba Medical Center

Locations

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Goldschleger Eye Institute

Tel Litwinsky, , Israel

Site Status RECRUITING

Countries

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Israel

Central Contacts

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Hani Levkovitch-Verbin, MD

Role: CONTACT

Facility Contacts

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Hani Levkovitch-Verbin, MD

Role: primary

Other Identifiers

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SHEBA-05-3876-HLV-CTIL

Identifier Type: -

Identifier Source: org_study_id

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