Ulnar Nerve Block for Procedural Anesthesia - Wrist Versus Palm
Recruitment status was Recruiting
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Purpose
Ulnar nerve blockade is necessary for sensory anesthesia and analgesia in the hand during minor procedures. The course of the ulnar nerve in the forearm, wrist, and hand is predictable and has low variability. However even with known anatomic location and landmarks, ulnar nerve blocks at the wrist frequently are inadequate for procedural anesthesia. The antebrachial fascia at the wrist acts as a barrier to local infiltration. Since the fascia can not be visualized or palpated, it is commonly is not penetrated, resulting in an inadequate block. Furthermore at the level of the wrist the ulnar artery lies in close proximity to the nerve and there is potential for arterial puncture while attempting injection for volar wrist block. The palmar ulnar nerve block is an injection distal to the hook of the hamate in the thenar eminence which avoids the ulnar artery and antebrachial fascia. This block has been used successfully for many years in clinical practice but has not been assessed or compared in a research study. The purpose of this study is to assess the validity of using a palmar ulnar nerve block for procedures in the hand as compared to the standard volar wrist ulnar nerve block.
| Condition | Intervention |
|---|---|
|
Hand Surgery |
Procedure: Local Block |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Efficacy Study Intervention Model: Single Group Assignment Masking: Single Blind (Investigator) Primary Purpose: Treatment |
| Official Title: | Ulnar Nerve Block for Procedural Anesthesia - Wrist Versus Palm |
- Primary outcome is efficacy of sensory anesthesia and analgesia [ Time Frame: 15-45 minutes ] [ Designated as safety issue: No ]
- Secondary outcome is patient perceived discomfort with block [ Time Frame: 15-45 Minutes ] [ Designated as safety issue: No ]
| Estimated Enrollment: | 246 |
| Study Start Date: | February 2008 |
| Estimated Study Completion Date: | December 2009 |
| Estimated Primary Completion Date: | December 2009 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Active Comparator: Hypothenar Palm block
Hypothenar Palmar block group. Local is placed at this location in this study arm. The same local composition (Intervention) is used for both study arms. The trial is a comparison of location not the Intervention.
|
Procedure: Local Block
total 3 cc injection (1.5 cc 1% plain lidocaine and 1.5 cc of 0.25% bupivicaine)
|
|
Active Comparator: Volar Wrist Block
Volar Wrist block group. Local is placed at this location in this study arm. The same local composition (Intervention) is used for both study arms. The trial is a comparison of location not the Intervention.
|
Procedure: Local Block
total 3 cc injection (1.5 cc 1% plain lidocaine and 1.5 cc of 0.25% bupivicaine)
|
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
- any individual who can give informed consent and is scheduled for elective hand procedures by the PI necessitating an Ulnar nerve block of the hand.
Exclusion Criteria:
- patients unable to give informed consent
- patients with previous or ongoing ulnar nerve deficits or neuropathy
- patients undergoing Guyon's canal decompression
- patients who can not comprehend or cooperate with assessment testing
- patients with abnormal two point discrimination (> 6 mm at the test location) prior to the nerve block
Contacts and Locations| Contact: Stuart Martin | 905-572-6226 | smartin@mcmaster.ca |
| Contact: Annika Card | 905-526-1948 | annika@quadrant.net |
| Canada, Ontario | |
| Hamilton General Hospital | Recruiting |
| Hamilton, Ontario, Canada | |
| Contact: Sonia Giangregorio-Campanella giangreg@hhsc.ca | |
| Principal Investigator: Stuart Martin | |
| Sub-Investigator: Annika Card | |
| Principal Investigator: | Stuart Martin | McMaster University |
More Information
No publications provided
| Responsible Party: | Dr. S. Martin, Division of Plastic Surgery, Department of Surgery, McMaster University |
| ClinicalTrials.gov Identifier: | NCT00827658 History of Changes |
| Other Study ID Numbers: | McMaster 08-053 |
| Study First Received: | January 21, 2009 |
| Last Updated: | January 22, 2009 |
| Health Authority: | Canada: Ethics Review Committee |
Keywords provided by McMaster University:
|
surgery, plastic anesthesia, local ulnar nerve hand blinded randomized |
prospective local anesthesia volar wrist block hypothenar palm block hand surgery |
Additional relevant MeSH terms:
|
Anesthetics Central Nervous System Depressants Physiological Effects of Drugs |
Pharmacologic Actions Central Nervous System Agents Therapeutic Uses |
ClinicalTrials.gov processed this record on May 16, 2013