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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03739086
Other study ID # ESPB-retro
Secondary ID
Status Completed
Phase
First received
Last updated
Start date July 1, 2017
Est. completion date November 14, 2018

Study information

Verified date November 2018
Source Maltepe University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Retrospective Evaluation of Erector Spinae Plane Blocks


Description:

in our institue; we use erector spinae plane block as a part of multimodal analjesia. we want to evaluate block failures and complications related erector spinae plane block. In all patients performed regional anesthesia techniques, we use a regional anesthesia follow chart.


Recruitment information / eligibility

Status Completed
Enrollment 182
Est. completion date November 14, 2018
Est. primary completion date November 1, 2018
Accepts healthy volunteers
Gender All
Age group N/A to 100 Years
Eligibility Inclusion Criteria:

- patient performed erector spinae plane block

Exclusion Criteria:

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
erector spinae plane block
unilateral or bilateral or bilevel erector spinae plane block performance for postoperative pain or acute pain

Locations

Country Name City State
Turkey Maltepe University faculty of medicine Istanbul

Sponsors (1)

Lead Sponsor Collaborator
Maltepe University

Country where clinical trial is conducted

Turkey, 

References & Publications (2)

Gürkan Y, Aksu C, Kus A, Yörükoglu UH, Kiliç CT. Ultrasound guided erector spinae plane block reduces postoperative opioid consumption following breast surgery: A randomized controlled study. J Clin Anesth. 2018 Nov;50:65-68. doi: 10.1016/j.jclinane.2018. — View Citation

Tsui BCH, Fonseca A, Munshey F, McFadyen G, Caruso TJ. The erector spinae plane (ESP) block: A pooled review of 242 cases. J Clin Anesth. 2018 Oct 3;53:29-34. doi: 10.1016/j.jclinane.2018.09.036. [Epub ahead of print] Review. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary complication rate 14 months
Secondary block failure rate 14 months
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