Efficacy of Subtenon's Block With Olive Tipped Cannula

The recruitment status of this study is unknown because the information has not been verified recently.
Verified November 2009 by King Khaled Eye Specialist Hospital.
Recruitment status was  Recruiting
Sponsor:
Information provided by:
King Khaled Eye Specialist Hospital
ClinicalTrials.gov Identifier:
NCT01019018
First received: November 17, 2009
Last updated: November 24, 2009
Last verified: November 2009

November 17, 2009
November 24, 2009
November 2009
April 2011   (final data collection date for primary outcome measure)
Measurement of Akinesia score [ Time Frame: 10 minutes after the block ] [ Designated as safety issue: No ]
Same as current
Complete list of historical versions of study NCT01019018 on ClinicalTrials.gov Archive Site
Surgeon satisfactions score [ Time Frame: At the end of the procedure ] [ Designated as safety issue: No ]
Same as current
Not Provided
Not Provided
 
Efficacy of Subtenon's Block With Olive Tipped Cannula
Efficacy of Subtenon Anesthesia With Olive Tipped Cannula: a Randomized Controlled Trial

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.

Not Provided
Interventional
Phase 4
Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Double Blind (Subject, Caregiver)
Primary Purpose: Health Services Research
Cataract
  • Device: subtenon block
    subtenon block with stevens cannula
  • Device: subtenon block
    subtenon block with Olive tip cannula cannula
  • Active Comparator: Stevens cannula
    Subtenon with stevens cannula
    Intervention: Device: subtenon block
  • Experimental: Olive tip
    Olive tip group
    Intervention: Device: subtenon block
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruiting
120
October 2011
April 2011   (final data collection date for primary outcome measure)

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.
Both
18 Years to 90 Years
No
Contact: Waleed Riad, MD,AB,SB,KSUF 0096614821234 ext 3215 waleed_riad@yahoo.com
Saudi Arabia
 
NCT01019018
RP 0928
Yes
Waleed Riad, King khaled Eye specialist hospital
King Khaled Eye Specialist Hospital
Not Provided
Not Provided
King Khaled Eye Specialist Hospital
November 2009

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP