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Clinical Trials/NCT03744520
NCT03744520
Completed
Not Applicable

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

Onur Selvi1 site in 1 country50 target enrollmentNovember 15, 2018
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ConditionsRegional Anesthesia Morbidity

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Regional Anesthesia Morbidity
Sponsor
Onur Selvi
Enrollment
50
Locations
1
Primary Endpoint
Spread of sensorial block
Status
Completed
Last Updated
6 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSitesSimilar Trials

Overview

Brief 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.

Registry
clinicaltrials.gov
Start Date
November 15, 2018
End Date
October 3, 2019
Last Updated
6 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
Onur Selvi
Responsible Party
Sponsor Investigator
Principal Investigator

Onur Selvi

MD

Maltepe University

Eligibility Criteria

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.

Outcomes

Primary Outcomes

Spread of sensorial block

Time Frame: in postoperative sixth hours

The sensorial block will be evaluated with dermatomal examination

Study Sites (1)

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