Anesthesia for Pars Plana Vitrectomy (PPV) With Insulin Needle - Tabular View

Tracking Information

First Received Date ^ICMJE

July 1, 2008

Last Updated Date

June 15, 2009

Start Date ^ICMJE

August 2008

Estimated Primary Completion Date

August 2009 (final data collection date for primary outcome measure)

Current Primary Outcome Measures ^ICMJE

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

Original Primary Outcome Measures ^ICMJE

Same as current

Change History

Complete list of historical versions of study NCT00735657 on ClinicalTrials.gov Archive Site

Current Secondary Outcome Measures ^ICMJE

Original Secondary Outcome Measures ^ICMJE

Descriptive Information

Brief Title ^ICMJE

Anesthesia for Pars Plana Vitrectomy (PPV) With Insulin Needle

Official Title ^ICMJE

Anesthesia for PPV Using Insulin Needle

Brief Summary

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

Detailed Description

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

Study Phase

Study Type ^ICMJE

Interventional

Study Design ^ICMJE

Treatment, Randomized, Single Blind (Investigator), Active Control, Parallel Assignment, Safety Study

Condition ^ICMJE

Retinal Disorders

Intervention ^ICMJE

Device: needle
Procedure: Pars Plana Vitrectomy

Study Arms / Comparison Groups

Active Comparator: Control
Active Comparator: Block with short needle

Publications *

* Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.

Recruitment Information

Recruitment Status ^ICMJE

Recruiting

Estimated Enrollment ^ICMJE

120

Estimated Completion Date

December 2010

Estimated Primary Completion Date

August 2009 (final data collection date for primary outcome measure)

Eligibility Criteria ^ICMJE

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

Gender

Both

Ages

40 Years and older

Accepts Healthy Volunteers

Contacts ^ICMJE

Contact: Waleed Riad, MD,AB,SB

0096614821234 ext 3215

waleed_riad@yahoo.com

Location Countries ^ICMJE

Saudi Arabia

Administrative Information

NCT ID ^ICMJE

NCT00735657

Responsible Party

Waleed Riad MD, King Khaled Eye Specialist Hospital

Study ID Numbers ^ICMJE

Rp0822

Study Sponsor ^ICMJE

King Khaled Eye Specialist Hospital

Collaborators ^ICMJE

Investigators ^ICMJE

Principal Investigator:

Waleed Riad, MD

KKESH

Information Provided By

King Khaled Eye Specialist Hospital

Verification Date

June 2009

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