Sensorial Block Assessment of Erector Spinae Block

Onur Selvi

Status: Completed

Conditions: Regional Anesthesia Morbidity

Treatments: Procedure: Erector spinae plane block

Study type: Interventional

Funder types: Other

Identifiers

NCT03744520

Sensorial Block assessment

Details and patient eligibility

About

Ultrasound-guided erector spinae plane blocks are used as postoperative analgesia method for abdominal, chest and hip surgeries. Regional techniques are well-described methods for postoperative analgesia. However, the sensorial dermatomal spread of regional block varies depending on the multiple variables as the level of the block, local analgesic concentration etc. The aim of this study is to observe dermatomal evaluation of sensorial block.

Enrollment: 50 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• The patients who received successful erector spinae plane block for postoperative analgesia

Exclusion criteria

• Patients under 18 years old
• Patients who are not able to communicate with
• Patients who are on medication which may change the perception of pain.

Trial design

Primary purpose: Screening

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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50 participants in 1 patient group

ESP block group

Experimental group

Description:

The patients who had paravertebral interfacial plane block for postoperative analgesia

Treatment:

Procedure: Erector spinae plane block