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Medial Cervical Block for Carotid Endarterectomy Comparison With Standard Method

A Comparison of Medial Cervical Plexus Block Versus Combined (Superficial and Deep) Cervical Plexus Block for Carotid Endarterectomy: A Prospective, Randomized Single Blind Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01608126
Enrollment
100
Registered
2012-05-30
Start date
2011-01-31
Completion date
2011-12-31
Last updated
2012-05-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cervical Plexus Block Comparison

Keywords

Ultrasound, Cervical Plexus, Anesthesia, Conduction, Surgical Procedures, Elective, Atherectomy

Brief summary

The purpose of the study is to compare efficacy, complications and safety of the standard method of Combined (superficial and deep) cervical plexus block (SDCPB) with Ultrasound guided Medial Cervical plexus block technique (MCPB). Hypothesis: Ultrasound assisted MCPB is safer than SDCPB with similar efficacy.

Interventions

PROCEDUREcervical block

In brief, the superficial block was performed using a 22G needle (07 x 40 mm). The mixture injected was 15 ml of 0.5% bupivacaine + 10 ml of 1% lidocaine. Deep cervical plexus block was performed using a Stimuplex DR stimulating needle and the dose of anaesthetic used was 10 ml 0.5% bupivacaine + 5 ml 1% lidocaine applied in the vicinity of the C3 nerve root. The MCPB performed using ultrasound-guidance aiming specifically for the interfascia space. Eighteen ml of 0.375% bupivacaine was injected into the interfascia space at the level of C3 vertebral body using a 22G needle (07 x 40 mm).

Sponsors

Daniel Nalos MD
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
30 Years to 90 Years
Healthy volunteers
No

Inclusion criteria

* Patients undergoing Elective Carotid Endarterectomy

Exclusion criteria

* Denied consent to block performance, Emergency procedure

Design outcomes

Primary

MeasureTime frameDescription
number of additional applications of short-acting local anaestheticintraoperativelyThe number of times a surgeon would have to supplement the Regional Block with intrafield application of increments of short-acting local anaesthetic
patient satisfaction24 h after operation
Complicationsperioperative

Countries

Czechia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026