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Effect of Two Different Plane Blocks on Post-thoracotomy Pain

Effects of Ultrasound-guided Continuous Erector Spina Plane Block and Continuous Serratus Anterior Plane Block on Post-thoracotomy Pain

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05083832
Enrollment
60
Registered
2021-10-19
Start date
2021-10-11
Completion date
2024-02-20
Last updated
2026-06-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Erector Spinae Plane Block, Pain, Postoperative, Serratus Anterior Plane Block, Thoracotomy

Keywords

Pain, Postoperative, Thoracotomy, Erector spinae plane block, Serratus anterior plane block

Brief 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.

Interventions

PROCEDUREContinuous Erector Spina Plane Block vs Continuous Serratus Anterior Plane Block

Two different catheter techniques with same doses local anesthetic infusion

Sponsors

Atatürk Chest Diseases and Chest Surgery Training and Research Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Pain scores72 hours after surgeryPain 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.

Secondary

MeasureTime frameDescription
Morphine consumption24 hours after surgeryMorphine consumption for 24 hours will be recorded
Side effects72 hours after surgerySide effects, such as allergy to local anesthetics, hypotension, nausea/vomiting, itching, headache, and sweating will be recorded.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 3, 2026