Comparison of the Rhomboid Intercostal Block and Serratus Posterior Superior Intercostal Plane Block

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-75
SponsorAnkara City Hospital Bilkent

About this trial

Video-assisted thoracic surgery (VATS) is widely performed for the management of various thoracic pathologies and is generally associated with reduced surgical trauma compared with open thoracotomy. Nevertheless, patients may still experience considerable postoperative pain, which can adversely affect respiratory function, mobilization, and recovery. Various regional analgesic techniques have been incorporated into multimodal pain management strategies for VATS, including thoracic paravertebral block (TPVB), erector spinae plane block (ESPB), intercostal nerve block, serratus anterior plane block (SAPB), rhomboid intercostal block (RIB), and serratus posterior superior intercostal plane block (SPSIPB). Among these approaches, ultrasound-guided TPVB has traditionally been regarded as a reference regional analgesic technique. More recently, interfascial plane blocks have gained increasing attention because of their technical simplicity and favorable safety profile. RIB and SPSIPB are two novel interfascial plane blocks that may provide effective postoperative analgesia following thoracic surgery. The present study aims to compare the analgesic efficacy of RIB and SPSIPB in patients undergoing VATS and to evaluate their impact on postoperative pain outcomes.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients undergoing elective VATS

Patients aged 18-75 years

Patients with ASA (American Society of Anesthesiologists) class I-III

Patients who have given informed consent

Disqualifiers

Patients allergic to local anesthetics

Patients with bleeding disorders or those undergoing anticoagulant therapy

Pregnant and breastfeeding women

Patients with impaired consciousness, inability to communicate, or mental/cognitive impairment

Trial design

Design model

Parallel

Treatments tested in this trial

  • Rhomboid Intercostal Block

    Drug

    Rhomboid intercostal block will be applied to the patients under real-time ultrasound guidance.

  • Serratus Posterior Superior Intercostal Plane Block

    Drug

    Serratus posterior superior intercostal plane block will be applied to the patients under real-time ultrasound guidance.

Treatment groups

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

Trial outcomes

Primary outcomes

1

Surgical Pain Scores

Surgical pain will be assessed at rest and while coughing using the visual analog scale on a scale from 0mm (no pain) to 100mm (worst pain). Pain assessment will be done at 1st, 6th, 12th, and 24th hours after surgery.

Time frame
24 hours after surgery

Secondary outcomes

1

Shoulder Pain Scores

Shoulder pain will be assessed at rest and while coughing using the visual analog scale on a scale from 0mm (no pain) to 100mm (worst pain). Pain assessment will be done at 1st, 6th, 12th, and 24th hours after surgery.

Time frame
24 hours after surgery
2

Intraoperative remifentanil consumption

The amount of remifentanil that patients need to maintain anesthesia during the intraoperative period will be recorded.

Time frame
During the intraoperative period

Other outcomes

Sponsors and contacts

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