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Clinical Trials/NCT02112006
NCT02112006
Completed
Not Applicable

A Comparison Of Distal Peripheral Nerve Blockade Versus Traditional Proximal Approaches For Hand Surgery

Jose Soberon, MD1 site in 1 country60 target enrollmentApril 2014

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Hand Injury
Sponsor
Jose Soberon, MD
Enrollment
60
Locations
1
Primary Endpoint
success of block
Status
Completed
Last Updated
10 years ago

Overview

Brief Summary

The purpose of this study is to compare two different injection sites for local anesthesia in patients having hand surgery. The hypothesis is that subjects receiving injections around the three nerves of the forearm will provide faster pain control and greater patient satisfaction than patients having one injection closer to the shoulder.

Registry
clinicaltrials.gov
Start Date
April 2014
End Date
March 2016
Last Updated
10 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
Jose Soberon, MD
Responsible Party
Sponsor Investigator
Principal Investigator

Jose Soberon, MD

Anesthesiologist

Ochsner Health System

Eligibility Criteria

Inclusion Criteria

  • Patients ≥ 18 years of age undergoing unilateral hand, wrist, or finger surgery
  • Ability to understand and provide informed consent
  • American Society of Anesthesiologists (ASA) status I-III

Exclusion Criteria

  • Patient refusal or inability to provide informed consent
  • True allergy, not sensitivity, to any of the following substances: Local Anesthetics, Midazolam, Fentanyl, Hydromorphone, Propofol
  • Pregnancy
  • Severe hepatic impairment
  • Evidence of infection at or near the proposed needle insertion site
  • Any sensorimotor deficit of the ipsilateral upper extremity, whether acute or chronic, as determined by the PI and designee
  • Pulmonary disease of any kind that is uncontrolled or severe in nature
  • Chronic pain patients, defined as someone diagnosed with chronic pain or a chronic pain condition, under the care of a chronic pain physician, or taking oral/intravenous narcotics consistently for 30 days prior to surgery

Outcomes

Primary Outcomes

success of block

Time Frame: up to 30 minutes after injection

number of participants that needed additional anesthesia

Secondary Outcomes

  • pain scores(up to 10 days after surgery)

Study Sites (1)

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