Rhomboid Intercostal and Subserratus Plane Block vs Erector Spinae Plane Block in Video-Assisted Thoracoscopic Surgery

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-80
SponsorBursa City Hospital

About this trial

To compare the rhomboid intercostal subserratus plane block with the erector spinae plane block regarding their analgesic efficacy and effects on respiratory function for patients undergoing video-assisted thoracoscopic surgery.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients who will undergo VATS

Who agrees to participate

American Society of Anesthesiologists (ASA) physical status I, II, and III

Elective surgery

Disqualifiers

Local anesthetic allergy

Who disagrees to participate

ASA physical status IV and V

Emergency surgery

Trial design

Design model

Parallel

Treatments tested in this trial

  • ESP block group

    Procedure/Surgery

    ESP blocks are performed for patients undergoing VATS.

  • RISS block group

    Procedure/Surgery

    RISS blocks are performed for patients undergoing VATS.

Treatment groups

90 Participants
are divided into 2 treatment groups
Group A: Patients who received ESP blockActive comparator 1 intervention
Group B: Patients who received RISS blockActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Opioid consumption

Total opioid consumption within the first 24 hours in the postoperative period.

Time frame
Postoperative first 24 hours.

Secondary outcomes

1

Dynamic pain score

Postoperative pain scores during coughing and deep breathing are measured on a 10 cm scale, where "0" indicates no pain and "10" indicates the worst pain ever.

Time frame
Postoperative first 24 hours.
2

Resting pain score

Postoperative pain scores during rest are measured on a 10 cm scale, where "0" indicates no pain and "10" indicates the worst pain ever.

Time frame
Postoperative first 24 hours.
3

Pulmonary functions

Pulmonary functions are assessed using Triflow performance. Postoperative Triflow numbers (whether 1, 2, or 3 balls can be raised) for the patients are recorded.

Time frame
Postoperative first 24 hours.
4

Complications

Complications regarding regional blocks and surgery (such as hematoma, pulmonary complications) are recorded.

Time frame
Through study completion, an average of 1 year

Other outcomes

Sponsors and contacts

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