Sensorial Block Assessment of Erector Spinae Block
Assessment of Dermatomal Sensorial Block of Erector Spinae Plane Block: Randomized, Prospective, Study
1 other identifier
interventional
50
1 country
1
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Nov 2018
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
October 25, 2018
CompletedStudy Start
First participant enrolled
November 15, 2018
CompletedFirst Posted
Study publicly available on registry
November 16, 2018
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 3, 2019
CompletedStudy Completion
Last participant's last visit for all outcomes
October 3, 2019
CompletedOctober 4, 2019
October 1, 2019
11 months
October 25, 2018
October 3, 2019
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Spread of sensorial block
The sensorial block will be evaluated with dermatomal examination
in postoperative sixth hours
Study Arms (1)
ESP block group
EXPERIMENTALThe patients who had paravertebral interfacial plane block for postoperative analgesia
Interventions
Local anesthetic infiltration is applied between the erector spinae muscle fascia and transverse process.
Eligibility Criteria
You may qualify if:
- The patients who received successful erector spinae plane block for postoperative analgesia
You may not qualify if:
- 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.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Onur Selvilead
Study Sites (1)
Maltepe University Medical Faculty
Istanbul, Maltepe, 34843, Turkey (Türkiye)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- SCREENING
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR INVESTIGATOR
- PI Title
- MD
Study Record Dates
First Submitted
October 25, 2018
First Posted
November 16, 2018
Study Start
November 15, 2018
Primary Completion
October 3, 2019
Study Completion
October 3, 2019
Last Updated
October 4, 2019
Record last verified: 2019-10
Data Sharing
- IPD Sharing
- Will not share