Comparison of Central Versus Peripheral Placement of Local Anesthetic

NCT ID: NCT00699244

Last Updated: 2017-06-12

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

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

218 participants

Study Classification

INTERVENTIONAL

Study Start Date

2006-12-31

Study Completion Date

2009-03-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

Does ultrasound increases the success rate and if there is a difference in success rate between placing the local anesthetic centrally versus peripherally.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

A comparison of the infraclavicular placement of local anesthetic either centrally (posterior cord) vs peripheral placement (lateral or medial cord) using ultrasound guidance. This will be done to determine if ultrasound increases the success rate and if there is a difference in success rate between placing the local anesthetic centrally versus peripherally.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Hand Surgery Elbow Surgery Forearm Surgery Wrist Surgery

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Peripheral placement of local anesthesia

to receive ultrasound guided peripheral placement of local anesthetic

Group Type EXPERIMENTAL

Peripheral placement of local anesthesia

Intervention Type PROCEDURE

Peripheral placement of local anesthesia

Central placement of local anesthesia

to receive central placement of local anesthetic

Group Type ACTIVE_COMPARATOR

Central placement of local anesthesia

Intervention Type PROCEDURE

Central placement of local anesthesia

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Peripheral placement of local anesthesia

Peripheral placement of local anesthesia

Intervention Type PROCEDURE

Central placement of local anesthesia

Central placement of local anesthesia

Intervention Type PROCEDURE

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* American Society of Anesthesiologists (ASA) Class I-III.
* Patient is undergoing elective hand or forearm surgery.
* Patient is an adult, 18 years old or older.

Exclusion Criteria

* Morbid obesity (calculated body mass index \> 35 kg/m2).
* Patient unable to cooperate.
* Patient with a known brachial plexus injury.
* Medical contraindication to anesthetic technique (allergy, cardiac condition, neurologic condition, localized infection, bleeding disorder).
* Patients who are pregnant.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Vanderbilt University

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Clifford Bowens

Assistant Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Clifford Bowens, M.D.

Role: PRINCIPAL_INVESTIGATOR

[email protected]

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Vanderbilt University Orthopedic Surgicenter

Nashville, Tennessee, United States

Site Status

Countries

Review the countries where the study has at least one active or historical site.

United States

Related Links

Access external resources that provide additional context or updates about the study.

http://www.vandydreamteam.com

Vanderbilt University Medical Center Department of Anesthesiology

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

61267

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.