Purpose

This study is being done to compare the two anesthesia techniques which are commonly used in the formation of arteriovenous fistulas: local anesthesia and regional anesthesia. Local anesthesia means that, your doctor will inject numbing medication directly into the tissue or part of your body where the surgery will be done. In this case, the numbing medication will be injected directly into the area where your fistula will be made. In regional anesthesia, the numbing medication will be injected around the nerve (part of the body that gives sensation) for your arm, to make the entire arm numb. The purpose of this study is to compare the three month success rates of AV fistulae created by the two anesthesia techniques.

Condition

Eligibility

Eligible Ages
Between 21 Years and 70 Years
Eligible Genders
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Age 21-70 years old - Able to give informed consent - Creation of first time AV fistula - Possible 3 month follow up visit - ASA-I-IV

Exclusion Criteria

  • BMI ≥40 - Repeated AV fistula creation, - ASA -V, - Allergic to local anesthetic agents, - Significant lung and cardiac disease, - Infection at the site of regional anesthesia, - Pre-existing peripheral nerve damage, - Significant bleeding disorders,

Study Design

Phase
N/A
Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel Assignment
Primary Purpose
Treatment
Masking
Single (Outcomes Assessor)

Arm Groups

ArmDescriptionAssigned Intervention
Active Comparator
Local anesthesia
  • Procedure: regional anesthesia
    Regional anesthesia will be compared to local anesthesia
Active Comparator
regional anesthesia
  • Procedure: local anesthesia
    Regional anesthesia will be compared to local anesthesia

More Details

Status
Terminated
Sponsor
Montefiore Medical Center

Study Contact

Detailed Description

The primary objectives of the study are: 1. To evaluate the three-month success rate for AV fistulas constructed while using regional anesthesia against those constructed while using local anesthesia. Success will be evaluated by a dialysis access ultrasound, which will be performed three months after completion of the procedure. Successful will be defined as a mean blood flow of 600 ml/min and above, or receiving hemodialysis using the newly created AV fistula. 2. To evaluate the immediate (within 3 days) and long-term complications three months after AV fistula construction under regional anesthesia or local anesthesia. The secondary objective of the study is to use a short questionnaire survey To assess patient comfort level after creation of AV fistula (e.g. nausea, analgesia).

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.