Cervical Plexus Block Combined With Translaryngeal Block for Tracheostomy

Namik Kemal University

Status: Completed

Conditions: Regional Anesthesia Morbidity

Treatments: Procedure: ST

Study type: Interventional

Funder types: Other

Identifiers

NCT04697836

Regional anesthesia

Details and patient eligibility

About

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 patients have difficulty in breathing, the more difficult it is to anaesthetize them. Adequate intraoperative anaesthesia and postoperative analgesia with minimal sedation play an essential role in this patient model. In tracheostomy patients, moving away from the general anaesthesia option increases airway safety, and avoiding the local anaesthesia option in the incision area increases patient comfort. The purpose of this study is to assess the safety and efficacy of regional anaesthesia in tracheostomy patients.

Full 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 computer-generated randomization list with a 1:1 intergroup ratio, ensuring equal distribution in the two groups, 30 opaque sealed envelopes numbered 1-30 were prepared. The patients were randomly divided into the Group with bilateral CPB with 15 ml 0.5% bupivacaine or the patients with translaryngeal block with 5 ml 2% lidocaine in addition to bilateral CPB.

CPB: cervical plexus block.

Enrollment: 29 patients

Sex: All

Ages: 18 to 65 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• 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 criteria

• 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.

Trial design

Primary purpose: Supportive Care

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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29 participants in 2 patient groups

ST (superficial cervical plexus block combined with Translareyngeal block)

Experimental group

Description:

Superficial cervical plexus block combined with Translareyngeal block Group.

Treatment:

Procedure: ST

S (superficial cervical plexus block)

Active Comparator group

Description:

Superficial cervical plexus block Group

Treatment:

Procedure: ST