ClinicalTrials.Veeva

Menu

Hemi-diaphragmatic Paresis After Erector Spinae Plane Block

A

Antalya Training and Research Hospital

Status

Terminated

Conditions

Carotid Endarterectomy
Regional Anesthesia

Treatments

Other: ESP block

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

To assess the incidence of hemi-diaphragmatic paresis following ultrasound-guided erector spinae plane (ESP) block

Full description

The ultrasound (USG) guided ESP block was first defined in 2016. With the administration of local anesthesia between the transverse process of the vertebra and the erector spinae muscle, it is stated that the effect mechanism of ESP is that spread blocks the ventral and dorsal rami to the paravertebral area. The aim of the study is to assess the incidence of hemi-diaphragmatic paresis following ultrasound-guided erector spinae plane block.

Enrollment

7 patients

Sex

All

Ages

18 to 85 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 18 - 85 years
  • American Society of Anesthesiology (ASA) I-III
  • elective carotid endarterectomy

Exclusion criteria

  • patient's refusal
  • under 18 years of age or over 65 years of age
  • ASA IV and above
  • known allergy to local anaesthetic drugs
  • the block cannot be applied due to bleeding disorders or localized skin infection at the injection site
  • history of neurological and/or neuromucular disease
  • history of severe bronchopulmonary disease
  • a moderate to severe decrease in preoperative pulmonary function, or abnormality in preoperative chest radiography data (pleural effusion, pneumothorax, or hemidiaphragm elevation)
  • emergency surgery

Trial design

7 participants in 1 patient group

ESP block group
Description:
Diaphragmatic excursion was measured using M-mode ultrasound during normal breathing, deep breathing and with the sniff manoeuvre.
Treatment:
Other: ESP block

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems