Actively Recruiting

Phase Not Applicable
Age: 40Years - 70Years
All Genders
NCT06419556

Analgesic Efficacy of an Intermediate CPB in Neck Surgeries.

Led by Cairo University · Updated on 2024-05-17

54

Participants Needed

1

Research Sites

64 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study aims to investigate the analgesic efficacy of Intermediate Cervical Plexus Block combined with GA using two bupivacaine concentrations in patients undergoing neck surgeries (total thyroidectomy or total laryngectomy)

CONDITIONS

Official Title

Analgesic Efficacy of an Intermediate CPB in Neck Surgeries.

Who Can Participate

Age: 40Years - 70Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients aged 40 to 70 years
  • ASA physical status I to III
  • Scheduled for total thyroidectomy or total laryngectomy under general anesthesia
Not Eligible

You will not qualify if you...

  • Heart failure
  • History of arrhythmias
  • Treatment with antiarrhythmic drugs
  • Impaired lung function
  • Impaired liver function
  • Impaired kidney function
  • Neck infection or rash

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Cairo university Hospitals. kasralainy

Cairo, Governorate, Egypt, 002

Actively Recruiting

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Research Team

N

Nagy malak

CONTACT

N

Nagy malak

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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