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The haemodynamic effect of superficial cervical plexus blockade in patients undergoing carotid endarterectomy under general anaesthesia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN52716583
Enrollment
54
Registered
2005-11-28
Start date
2005-11-20
Completion date
Unknown
Last updated
2015-01-13

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

Conditions

Blood pressure lability Signs and Symptoms Abnormal blood pressure reading

Interventions

Patients will receive a superfical cervical plexus block with either 2 mg/kg of laevo-bupivacaine or a placebo block with the equivalent volume of saline

Sponsors

James Cook University Hospital (UK)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients at James Cook University Hospital undergoing carotid endartectomy

Exclusion criteria

Exclusion criteria: Patients will be excluded if they: 1. Do not wish to take part 2. Are unfit for a general anaesthetic 3. Have a contraindication to either beta blockers or to being given a local anaesthetic block (e.g. local anaesthetic allergy and bleeding tendency)

Design outcomes

Primary

MeasureTime frame
Mean systolic blood pressures over the first 24 hours postoperatively.

Secondary

MeasureTime frame
1. Need for antihypertensive treatment 2. Need for pressor treatment 3. Cumulative dose of any vasoactive medication 4. Mean pain scores 5. Cumulative opiate requirements Any cardiovascular, cerebrovascular or other major morbidity or mortality occuring during the time period and any complication potentially related to the superficial cervical plexus block will also be recorded.

Countries

United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026