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NCT03744520 Clinical Trial

Sensorial Block Assessment of Erector Spinae Block

Regional Anesthesia Morbidity Clinical Trial

Official title:
Assessment of Dermatomal Sensorial Block of Erector Spinae Plane Block: Randomized, Prospective, Study

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03744520
Other study ID # Sensorial Block assessment
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date November 15, 2018
Est. completion date October 3, 2019

Study information
Verified date October 2019
Source Maltepe University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.

Recruitment information / eligibility
Status Completed
Enrollment 50
Est. completion date October 3, 2019
Est. primary completion date October 3, 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility 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.

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• Erector spinae plane block
Local anesthetic infiltration is applied between the erector spinae muscle fascia and transverse process.

Locations
Country Name City State
Turkey Maltepe University Medical Faculty Istanbul Maltepe

Sponsors (1)
Lead Sponsor Collaborator
Onur Selvi

Country where clinical trial is conducted

Turkey, 

Outcome
Type Measure Description Time frame Safety issue
Primary Spread of sensorial block The sensorial block will be evaluated with dermatomal examination in postoperative sixth hours
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