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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05083832
Other study ID # E.Kurul-E1-21-1863
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date June 9, 2021
Est. completion date February 20, 2024

Study information

Verified date March 2024
Source Atatürk Chest Diseases and Chest Surgery Training and Research Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Thoracotomy is recognized as one of the most painful surgical procedures. This increases the frequency of postoperative pulmonary complications. Erector Spinae Plane Block (ESPB) and Serratus Anterior Plane Block (SAPB) are more superficial, easier to perform, and less likely to have complications. In addition, ESPB and SAPB applications are increasing in patients who underwent thoracotomy and thoracoscopic surgery. In this study, the investigators aimed to evaluate the effect of continuous ESPB and continuous SAPB via US-guidance on post-thoracotomy pain.


Recruitment information / eligibility

Status Completed
Enrollment 60
Est. completion date February 20, 2024
Est. primary completion date January 9, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: - 18 to 65 years old - ASA physical status I-II-III - BMI 18 to 30 kg/m2 - Elective thoracotomy surgery Exclusion Criteria: - Patient refusing the procedure - Emergency surgery - History of chronic opioid or analgesic used

Study Design


Intervention

Procedure:
Continuous Erector Spina Plane Block vs Continuous Serratus Anterior Plane Block
Two different catheter techniques with same doses local anesthetic infusion

Locations

Country Name City State
Turkey Ankara Atatürk Chest Disease and Chest Surgery Training and Research Hospital Kecioren Ankara

Sponsors (1)

Lead Sponsor Collaborator
Atatürk Chest Diseases and Chest Surgery Training and Research Hospital

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Pain scores Pain will be assessed at rest and while coughing using the visual analog scale on a scale from 0 (no pain) to 10 (worst pain). Pain assessment will be done at 1st, 2nd, 4th, 8th, 16th, 24th, 48th and 72nd hours after surgery. 72 hours after surgery
Secondary Morphine consumption Morphine consumption for 24 hours will be recorded 24 hours after surgery
Secondary Side effects Side effects, such as allergy to local anesthetics, hypotension, nausea/vomiting, itching, headache, and sweating will be recorded. 72 hours after surgery
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