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Erector Spinae Plane Block for Carotid Endarterectomy

A

Antalya Training and Research Hospital

Status

Suspended

Conditions

Pain

Treatments

Other: Control group
Other: Erector spinae plane block

Study type

Interventional

Funder types

Other

Identifiers

NCT04224844
AntalyaTRH029

Details and patient eligibility

About

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.

Full 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.

Enrollment

34 estimated patients

Sex

All

Ages

18 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients undergoing carotid endarterectomy
  • American Society of Anesthesiologists class 2 to 3
  • Ability to consent

Exclusion criteria

  • inability to communicate
  • not understand the aim and objectives of the study
  • not provide informed written consent
  • contraindications for the block (local infection, coagulation disorders)
  • hypersensitivity to the local anesthetics
  • refusal of regional anesthesia

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

34 participants in 2 patient groups

Erector spinae plane block group (Group 1)
Active Comparator group
Description:
Patients will receive erector spinae plane block in addition to intravenous patient-controlled analgesia device containing tramadol.
Treatment:
Other: Erector spinae plane block
Control group (Group 2)
Active Comparator group
Description:
Control group will receive only intravenous patient-controlled analgesia device containing tramadol.
Treatment:
Other: Control group

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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