Anesthesia for Pars Plana Vitrectomy (PPV) With Insulin Needle

NCT ID: NCT00735657

Last Updated: 2021-12-02

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

120 participants

Study Classification

INTERVENTIONAL

Study Start Date

2008-08-31

Study Completion Date

2010-12-31

Brief Summary

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

Detailed Description

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

Conditions

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Retinal Disorders

Keywords

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Efficiency Pars Plana Vitrectomy

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Investigators

Study Groups

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Group 1

Control

Group Type ACTIVE_COMPARATOR

needle

Intervention Type DEVICE

Peribulbar blockade with standard (25 mm) needle

Pars Plana Vitrectomy

Intervention Type PROCEDURE

Peribulbar block

Group 2

Block with short needle

Group Type ACTIVE_COMPARATOR

needle

Intervention Type DEVICE

Peribulbar blockade with short (12.5 mm) needle

Pars Plana Vitrectomy

Intervention Type PROCEDURE

Peribulbar block

Interventions

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needle

Peribulbar blockade with standard (25 mm) needle

Intervention Type DEVICE

needle

Peribulbar blockade with short (12.5 mm) needle

Intervention Type DEVICE

Pars Plana Vitrectomy

Peribulbar block

Intervention Type PROCEDURE

Other Intervention Names

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Peribulbar blockade with standard needle Peribulbar blockade with short needle Extraconal block

Eligibility Criteria

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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
Minimum Eligible Age

40 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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King Khaled Eye Specialist Hospital

OTHER_GOV

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Waleed Riad, MD

Role: PRINCIPAL_INVESTIGATOR

KKESH

Locations

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King Khaled Eye Specialist hospital

Riyadh, , Saudi Arabia

Site Status

Countries

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Saudi Arabia

Other Identifiers

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Rp0822

Identifier Type: -

Identifier Source: org_study_id