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Anesthesia for Pars Plana Vitrectomy (PPV) With Insulin Needle

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ClinicalTrials.gov Identifier: NCT00735657
Recruitment Status : Unknown
Verified February 2010 by King Khaled Eye Specialist Hospital.
Recruitment status was:  Recruiting
First Posted : August 15, 2008
Last Update Posted : February 25, 2010
Sponsor:
Information provided by:
King Khaled Eye Specialist Hospital

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

Condition or disease Intervention/treatment Phase
Retinal Disorders Device: needle Procedure: Pars Plana Vitrectomy Not Applicable

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

Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 120 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Single (Investigator)
Primary Purpose: Treatment
Official Title: Anesthesia for PPV Using Insulin Needle
Study Start Date : August 2008
Estimated Primary Completion Date : August 2009
Estimated Study Completion Date : December 2010

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Anesthesia

Arm Intervention/treatment
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




Primary Outcome Measures :
  1. Efficacy of insulin needle. [ Time Frame: 1 year ]


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Ages Eligible for Study:   40 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
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

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): 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

Responsible Party: Waleed Riad MD, King Khaled Eye Specialist Hospital
ClinicalTrials.gov Identifier: NCT00735657     History of Changes
Other Study ID Numbers: Rp0822
First Posted: August 15, 2008    Key Record Dates
Last Update Posted: February 25, 2010
Last Verified: February 2010

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

Additional relevant MeSH terms:
Retinal Diseases
Eye Diseases
Temazepam
Hypnotics and Sedatives
Central Nervous System Depressants
Physiological Effects of Drugs
Anti-Anxiety Agents
Tranquilizing Agents
Psychotropic Drugs
GABA Modulators
GABA Agents
Neurotransmitter Agents
Molecular Mechanisms of Pharmacological Action