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Efficacy of Subtenon's Block With Olive Tipped Cannula

The recruitment status of this study is unknown. The completion date has passed and the status has not been verified in more than two years.
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
No Changes Posted
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.
 
Unknown status
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   (Adult, Senior)
No
Contact information is only displayed when the study is recruiting subjects
Saudi Arabia
 
NCT01019018
RP 0928
Yes
Not Provided
Not Provided
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