Anesthesia for Pars Plana Vitrectomy (PPV) With Insulin Needle

The recruitment status of this study is unknown because the information has not been verified recently.
Verified February 2010 by King Khaled Eye Specialist Hospital.
Recruitment status was  Recruiting
Sponsor:
Information provided by:
King Khaled Eye Specialist Hospital
ClinicalTrials.gov Identifier:
NCT00735657
First received: July 1, 2008
Last updated: February 24, 2010
Last verified: February 2010
  Purpose

Periocular blockade with 12.5 mm needle is as effective as block with 25 mm needle for patients undergoing Pars Plana Vitrectomy.


Condition Intervention
Retinal Disorders
Device: needle
Procedure: Pars Plana Vitrectomy

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Safety Study
Intervention Model: Parallel Assignment
Masking: Single Blind (Investigator)
Primary Purpose: Treatment
Official Title: Anesthesia for PPV Using Insulin Needle

Resource links provided by NLM:


Further study details as provided by King Khaled Eye Specialist Hospital:

Primary Outcome Measures:
  • Efficacy of insulin needle. [ Time Frame: 1 year ] [ Designated as safety issue: Yes ]

Estimated Enrollment: 120
Study Start Date: August 2008
Estimated Study Completion Date: December 2010
Estimated Primary Completion Date: August 2009 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Active Comparator: Group 1
Control
Device: needle
Peribulbar blockade with standard (25 mm) needle
Other Name: Peribulbar blockade with standard needle
Procedure: Pars Plana Vitrectomy
Peribulbar block
Other Name: Extraconal block
Active Comparator: Group 2
Block with short needle
Device: needle
Peribulbar blockade with short (12.5 mm) needle
Other Name: Peribulbar blockade with short needle
Procedure: Pars Plana Vitrectomy
Peribulbar block
Other Name: Extraconal block

Detailed Description:

The author wants to see the effect of short needle in patients undergoing retinal surgery.

  Eligibility

Ages Eligible for Study:   40 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Adult patients undergoing pars plana vitrectomy under local anesthesia

Exclusion Criteria:

  • Patients allergic to local anesthetic solutions
  • With local sepsis
  • Serious impairment of coagulation
  • Orbital abnormalities
  • Unable to cooperate in maintaining a relatively motionless supine position
  • Who refused the anesthetic technique
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00735657

Contacts
Contact: Waleed Riad, MD,AB,SB 0096614821234 ext 3215 waleed_riad@yahoo.com

Locations
Saudi Arabia
King Khaled Eye Specialist hospital Recruiting
Riyadh, Saudi Arabia, 11462
Contact: Waleed Riad    0096614821234 ext 3215    waleed_riad@yahoo.com   
Principal Investigator: Waleed Riad, MD, AB,SB         
Sponsors and Collaborators
King Khaled Eye Specialist Hospital
Investigators
Principal Investigator: Waleed Riad, MD KKESH
  More Information

No publications provided

Responsible Party: Waleed Riad MD, King Khaled Eye Specialist Hospital
ClinicalTrials.gov Identifier: NCT00735657     History of Changes
Other Study ID Numbers: Rp0822
Study First Received: July 1, 2008
Last Updated: February 24, 2010
Health Authority: Saudi Arabia: Ministry of Health

Keywords provided by King Khaled Eye Specialist Hospital:
Efficiency
Pars
Plana
Vitrectomy

Additional relevant MeSH terms:
Retinal Diseases
Eye Diseases

ClinicalTrials.gov processed this record on October 21, 2014