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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02714738
Other study ID # TP-ICB-ABPB
Secondary ID
Status Completed
Phase N/A
First received March 16, 2016
Last updated August 19, 2017
Start date March 2016
Est. completion date May 9, 2017

Study information

Verified date August 2017
Source Cork University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to determine whether the incidence of tourniquet pain is decreased if infraclavicular nerve block is administered, compared to axillary brachial plexus block, for surgical interventions at the level or distal to the elbow.


Description:

Pneumatic tourniquets are often used in orthopedic surgery to ensure bloodless surgical field. Besides their obvious positive effects, arterial tourniquets have some unfavorable properties. One of these is tourniquet pain, which can manifest in the presence of an otherwise adequate neuraxial or peripheral nerve block. If it develops, it is usually difficult to manage, and can be severe enough to necessitate conversion to general anaesthesia.

In the past the incidence of tourniquet pain, associated with different nerve blocks has been estimated in clinical trials for which it was a secondary outcome measure. One recent meta-analysis addressed the question: is infraclavicular block (ICB) associated with a lesser incidence of tourniquet pain compared to other brachial plexus blocks. The studies selected by this meta-analysis used different types of nerve block. However it did not address the clinically relevant question: using standard techniques for ultrasound guided brachial plexus block (USgBPB) is the infraclavicular approach associated with a lesser incidence of tourniquet pain than the axillary approach? The following nerves contribute to the perception of tourniquet pain: musculocutaneous, radial, medial cutaneous brachial (MCBN) and intercostobrachial (ICBN). The potential advantage of the ICB over the axillary brachial plexus block (ABPB) in regards to tourniquet pain comes from anatomical reasons. In the pyramid shaped infraclavicular space the cords are much closer to each other; thus the likelihood of achieving effective MCBN and ICBN block is greater. The infraclavicular route has proven to result in an equally effective, reliable and safe block of the brachial plexus, compared to the axillary approach. We hypothesize that the incidence of tourniquet pain is less with infraclavicular block compared to axillary brachial plexus block.

The aim of the study is, to compare the incidence and severity of tourniquet pain associated with ultrasound guided ICB and ABPB in patients undergoing orthopedic surgery at the level or distal to the elbow, with a tourniquet time longer than 45 minutes.


Recruitment information / eligibility

Status Completed
Enrollment 82
Est. completion date May 9, 2017
Est. primary completion date May 9, 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- ASA I-III

- Orthopedic surgery at the level or distal to the elbow

- Expected tourniquet time > 45 min (K-wiring not suitable)

Exclusion Criteria:

- Contraindication of regional anaesthesia, patient is allergic to local anesthetics

- Clinically significant cognitive impairment (Minimental state score < 24)

- Chronic pain syndrome

- Preexisting nerve damage in the operated arm (sensory or motor deficit)

- Axillary clearance in the past

- History of peripheral neuropathy)

- Pregnancy

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Ultrasound guided peripheral nerve block
Ultrasound guided peripheral nerve block

Locations

Country Name City State
Ireland Division of Anaesthesia and Intensive Care, Cork University Hospital Cork Co. Cork

Sponsors (1)

Lead Sponsor Collaborator
Cork University Hospital

Country where clinical trial is conducted

Ireland, 

References & Publications (4)

Chin KJ, Alakkad H, Adhikary SD, Singh M. Infraclavicular brachial plexus block for regional anaesthesia of the lower arm. Cochrane Database Syst Rev. 2013 Aug 28;(8):CD005487. doi: 10.1002/14651858.CD005487.pub3. Review. — View Citation

Estebe JP, Davies JM, Richebe P. The pneumatic tourniquet: mechanical, ischaemia-reperfusion and systemic effects. Eur J Anaesthesiol. 2011 Jun;28(6):404-11. doi: 10.1097/EJA.0b013e328346d5a9. Review. — View Citation

Kam PC, Kavanagh R, Yoong FF. The arterial tourniquet: pathophysiological consequences and anaesthetic implications. Anaesthesia. 2001 Jun;56(6):534-45. Review. Erratum in: Anaesthesia 2001 Aug;56(8):821. Kavanaugh R [corrected to Kavanagh R]. — View Citation

Sauter AR, Smith HJ, Stubhaug A, Dodgson MS, Klaastad Ø. Use of magnetic resonance imaging to define the anatomical location closest to all three cords of the infraclavicular brachial plexus. Anesth Analg. 2006 Dec;103(6):1574-6. Erratum in: Anesth Analg. 2007 Mar;104(3):562. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Incidence of tourniquet pain Intraoperative period
Secondary Onset time of tourniquet pain Intraoperative period
Secondary Severity of tourniquet pain Mild tourniquet pain (no need for intervention*) Moderate tourniquet pain (need for fentanyl / additional sedation*) Severe tourniquet pain (requiring GA*)
*: based on the clinical judgement of the responsible clinician (not a member of the study team)
Intraoperative period
Secondary Incidence of adverse events Vascular puncture or paresthesia during block placement During block placement
Secondary Block performance time From commencing sterile preparation to completion of injection of local anaesthetic During block placement
Secondary Block onset time From completed injection of local anaesthetic until loss of cold sensation in distribution of radial, ulnar, median and musculocutaneous nerve in the hand and forearm 30 minutes after block placement
Secondary Incidence of block failure Presence of cold sensation in at least one distribute of radial, ulnar, median and musculocutaneous nerves in the hand and forearm at 30 min after completion of injection of local anaesthetic 30 minutes after block placement
See also
  Status Clinical Trial Phase
Not yet recruiting NCT03357055 - Ketamine Reduces Tourniquet Pain In Patients Undergoing Lower Limb Surgery Under Spinal Anaesthesia Phase 4
Recruiting NCT05602636 - Analgesic Effect of Supraclavicular Block and Interscalene Analgesia Versus an Intercostobrachial Nerve Block Versus PCA in Forearm Surgery Phase 4
Completed NCT05342870 - A Sequential Allocation Study to Determine the ED50 of Dexmetedomidine as an Adjuvant to Lidocaine Intravenous Regional Anesthesia N/A