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NCT Number: NCT07650877

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

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.

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Ankara City Hospital

Çankaya, Ankara, 06290, Turkey (Türkiye)

Location status: Recruiting

Location contact

Emine N Zengin, MD

CONTACT

[email protected]

+905063370548

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 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

Exclusion criteria

  • 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
  • Patients who refuse block application
  • Patients with infection in the area where the block will be applied

Treatment and study plan

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.

Primary outcomes

  1. Surgical Pain Scores

    Time frame: 24 hours after surgery

    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.

Secondary outcomes

  1. Shoulder Pain Scores

    Time frame: 24 hours after surgery

    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.

  2. Intraoperative remifentanil consumption

    Time frame: During the intraoperative period

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

Study contacts

Contact information is provided by the study sponsor or research team.

Emine Nilgün Zengin, Associate Professor

CONTACT

[email protected]

00905063370548

Hülya Yiğit, Associate Professor

CONTACT

[email protected]

00905054853939

Sponsors and collaborators

Lead sponsor

Ankara City Hospital Bilkent

Other

Registry information

Official study title

Comparison of the Effects of Ultrasound-Guided Rhomboid Intercostal Block and Serratus Posterior Superior Intercostal Plane Block on Postoperative Acute Pain in Patients Undergoing Video-Assisted Thoracoscopic Surgery

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Jun 16, 2026
Registry last updated
Jun 16, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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