Clinical Trials Directory

Trials / Suspended

SuspendedNCT04224844

Erector Spinae Plane Block for Carotid Endarterectomy

Ultrasound-Guided Spinae Plane Block for Perioperative Pain Control in Carotid Endarterectomy.

Status
Suspended
Phase
N/A
Study type
Interventional
Enrollment
34 (estimated)
Sponsor
Antalya Training and Research Hospital · Other Government
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to test the hypothesis that erector spinae plane block will decrease intraoperative local anesthetic and postoperative analgesic consumption in patients undergoing carotid endarterectomy.

Detailed description

Patients who decided to participate in the study will be randomized into 2 groups: Erector Spinae Plane Block Group (Group E) and Control Group (Group C). Intraoperative local anesthetic consumption, postoperative tramadol consumption, intraoperative and pain scores, hemodynamic parameters and patient satisfaction will be recorded.

Conditions

Interventions

TypeNameDescription
OTHERErector spinae plane blockThe block will be performed before the surgery. The spinous process of T2 or T3 wil be identified by an ultrasound guide, with the probe positioned longitudinally. A block needle will be inserted in the caudo-cephal direction. After the injection site is confirmed by 3 ml of physiological solution and correct position of the needle tip is confirmed, bupivacaine will be injected. The patients assigned to this group will also receive an intravenous patient-controlled analgesia device containing tramadol postoperatively.
OTHERControl groupControl group will receive only patient-controlled analgesia device containing tramadol. No block will be performed.

Timeline

Start date
2020-09-01
Primary completion
2020-12-01
Completion
2021-02-01
First posted
2020-01-13
Last updated
2020-04-30

Locations

1 site across 1 country: Turkey (Türkiye)

Source: ClinicalTrials.gov record NCT04224844. Inclusion in this directory is not an endorsement.