Postoperative Analgesic Comparison of SPSI Block and SAP Block in Video-Assisted Thoracoscopic Surgery (VATS)

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-80
SponsorUludag University

About this trial

In our study, we primarily aimed to compare the postoperative analgesic effectiveness of the Serratus Posterior Superior Intercostal Plane Block and the Serratus Anterior Plane Block, both routinely applied in patients undergoing Video-Assisted Thoracoscopic Surgery (VATS)

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Patients aged 18 to 80 years undergoing Video-Assisted Thoracoscopic Surgery (VATS)

Scheduled at Uludağ University Faculty of Medicine Hospital Operating Room

Classified as ASA I, II, or III according to the American Society of Anesthesiologists (ASA) criteria

Disqualifiers

Allergy to local anesthetics or contraindications to bupivacaine

Known or suspected coagulopathy

Infection at the injection site

History of thoracic surgery

Trial design

Design model

Parallel

Treatments tested in this trial

  • Serratus Posterior Superior Intercostal Plane Block

    Procedure/Surgery

    Patients undergoing Video-Assisted Thoracoscopic Surgery (VATS) will receive either a Serratus Posterior Superior Intercostal Plane Block (SPSIPB) with bupivacaine after induction and before the surgical procedure begins.

  • Serratus Anterior Plane Block

    Procedure/Surgery

    Patients undergoing Video-Assisted Thoracoscopic Surgery (VATS) will receive either a Serratus Anterior Plane Block (SAPB) with bupivacaine after induction and before the surgical procedure begins.

Treatment groups

90 Participants
are divided into 2 treatment groups
Group A: Serratus Posterior Superior Intercostal Plane Block GroupActive comparator 1 intervention
Group B: Serratus Anterior Plane Block GroupActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

The Numerical Rating Scale (NRS)

Numerical Rating Scale (NRS) The Numerical Rating Scale (NRS) is a commonly used pain assessment tool that allows patients to rate their pain intensity on a scale from 0 to 10. 0 indicates no pain. 10 indicates the worst possible pain. Patients are asked to choose a number that best represents their pain level at the time of assessment.

Time frame
2 days

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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