Status:

COMPLETED

Cervical Plexus Block Combined With Translaryngeal Block for Tracheostomy

Lead Sponsor:

Namik Kemal University

Conditions:

Regional Anesthesia Morbidity

Eligibility:

All Genders

18-65 years

Phase:

NA

Brief Summary

Current healthcare delivery models emphasize enhanced postoperative recovery (ERAS) with minimal morbidity and shorter hospital stays. Most tracheostomy cases are tumour patients. The more the patient...

Detailed Description

after being informed and about the study and potential risks, all patients giving written informed consent will undergo 24 hours screening period to determine the eligilibity for study entry. After a ...

Eligibility Criteria

Inclusion

  • Being in the age range of 18-65, with American Society of Anesthesiology (ASA) classification I-III and scheduled for elective or emergency tracheostomy.
  • A sufficient level of education to understand the study procedures and agree to participate in the study

Exclusion

  • inability to cooperate
  • dementia,
  • allergy to local anesthetics and opioids
  • regular daily opioid requirements
  • abuse of alcohol or medication
  • local infection at the site of injection or systemic infection,
  • pregnancy.

Key Trial Info

Start Date :

March 1 2020

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

November 25 2020

Estimated Enrollment :

29 Patients enrolled

Trial Details

Trial ID

NCT04697836

Start Date

March 1 2020

End Date

November 25 2020

Last Update

January 6 2021

Active Locations (1)

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Namık Kemal University

Tekirdağ, Süleymanpaşa, Turkey (Türkiye), 59100