CompletedN/AOther

Bilateral Erector Spinae Plane Block for Postoperative Chronic Pain After Open Heart Surgery

Sponsored by Ondokuz Mayıs University

NCT ID
NCT06315959
Target Enrollment
71 participants
Start Date
2024-04-01
Est. Completion
2025-02-20

About This Study

The aim of this study is to investigate the effect of bilateral erector spinae plane (ESP) block application on postoperative chronic pain in patients undergoing on-pump open-heart surgery. At 3 months post-discharge, patients will be contacted by phone to assess their chronic pain status. Pain intensity and status will be evaluated using the Brief Pain Inventory, and the character of pain will be assessed using the Douleur Neuropathique 4 (DN4) score. Additionally, the patient's anxiety and depression status will be evaluated using the Hospital Anxiety and Depression Scale.

Conditions Studied

Chronic PainCardiac SurgeryPost Operative Pain

Interventions

  • Bilateral ultrasound guided erector spinae plane block
  • morphine PCA
  • Control group
  • morphine PCA

Eligibility

Age:18 Years - 80 Years
Healthy Volunteers:No
View full eligibility criteria
Inclusion Criteria:

* Patients aged 18-80 undergoing elective on-pump open-heart surgery via median sternotomy.
* American Society of Anesthesiologists (ASA)classification II-III patients.
* Patients who can use PCA.
* Patients who will sign the informed consent form.

Exclusion Criteria:

* History of opioid use for more than four weeks
* Chronic pain syndromes
* Patients with a history of local anesthetic or opioid allergy, hypersensitivity
* Alcohol and drug addiction
* Conditions where regional anesthesia is contraindicated
* Failure in the dermatomal examination performed after the block
* Emergency surgeries and redo surgeries.
* Individuals with obstructive sleep apnea.
* Left ventricular ejection fraction less than 30%.
* Patients with severe psychiatric illnesses (such as psychosis, dementia) that limit cooperation with verbal numerical pain scales.
* Pregnant and breastfeeding patients.
* Hematological disorders.
* Significant impairment in the function of a major organ (e.g., severe hepatic or renal disease).
* Patients who cannot be extubated within the first 6 hours postoperatively.

Study Locations (1)

Ondokuz Mayis University
Samsun, Atakum, Turkey (Türkiye)

This trial is not recruiting

This study has completed enrollment. Check back for results or find similar trials.

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Data Source
ClinicalTrials.gov

Last updated from source

Bilateral Erector Spinae Plane Block for Postoperative Chronic Pain After Open Heart Surgery | Huxley