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NCT01019018 Clinical Trial

Efficacy of Subtenon's Block With Olive Tipped Cannula

Cataract Clinical Trial

Official title:
Efficacy of Subtenon Anesthesia With Olive Tipped Cannula: a Randomized Controlled Trial

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01019018
Other study ID # RP 0928
Secondary ID
Status Completed
Phase Phase 4
First received
Last updated
Start date November 2009
Est. completion date October 2011

Study information
Verified date November 2009
Source King Khaled Eye Specialist Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to compare the efficacy of olive tip cannula to the standard Steven's cannula in performing subtenon's anesthesia for patients undergoing cataract surgery.

Recruitment information / eligibility
Status Completed
Enrollment 120
Est. completion date October 2011
Est. primary completion date April 2011
Accepts healthy volunteers No
Gender All
Age group 18 Years to 90 Years
Eligibility Inclusion Criteria: - Patient undergoing cataract extraction procedure under local anesthesia Exclusion Criteria: - Patients allergic to local anesthetic solutions. - Presence local sepsis, - Previous retinal or strabismus surgery in the same eye. - Orbital abnormalities - Previous subtenon's block in the same quadrant.

Study Design

Related Conditions & MeSH terms

Intervention

Device:
• subtenon block
subtenon block with stevens cannula
• subtenon block
subtenon block with Olive tip cannula cannula

Locations
Country Name City State
Saudi Arabia king Khaled Eye Specialist hospital Riyadh

Sponsors (1)
Lead Sponsor Collaborator
King Khaled Eye Specialist Hospital

Country where clinical trial is conducted

Saudi Arabia, 

Outcome
Type Measure Description Time frame Safety issue
Primary Measurement of Akinesia score 10 minutes after the block
Secondary Surgeon satisfactions score At the end of the procedure
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