Timing of Subcostal TAPB Combined With Rectus Sheath Block for Postoperative Pain After Laparoscopic Cholecystectomy

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-80
SponsorEulji University Hospital

About this trial

This prospective randomized controlled trial aims to evaluate whether the timing of ultrasound-guided subcostal transversus abdominis plane (TAP) block combined with rectus sheath block (RSB) affects postoperative pain in patients undergoing laparoscopic cholecystectomy.

Participants will be randomly assigned to receive the combined regional blocks either before surgical incision or after completion of surgery. The primary outcome is postoperative pain intensity measured using a numerical rating scale. Secondary outcomes include opioid consumption, incidence of postoperative nausea and vomiting, and other recovery parameters.

The results of this study may help optimize the timing of abdominal wall blocks to improve postoperative analgesia and recovery following laparoscopic cholecystectomy.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Elective laparoscopic cholecystectomy

Adults aged 18 to 80 years

Ability to understand the study procedures and provide informed consent

American Society of Anesthesiologists (ASA) physical status I-III

Disqualifiers

Presence of significant pain unrelated to the target disease that may interfere with pain assessment

Known allergy or contraindication to study medications (ropivacaine, acetaminophen, nefopam, or pethidine)

Planned single-port laparoscopic cholecystectomy

American Society of Anesthesiologists (ASA) physical status IV or higher

Trial design

Design model

Parallel

Treatments tested in this trial

  • Ultrasound-guided subcostal TAP block combined with rectus sheath block

    Procedure/Surgery

    Ultrasound-guided right subcostal transversus abdominis plane (TAP) block combined with bilateral rectus sheath block (RSB) is performed under sterile conditions using local anesthetic for postoperative analgesia.

Treatment groups

96 Participants
are divided into 2 treatment groups
Group A: Pre-incisional Block GroupExperimental treatment 1 intervention
Group B: Postoperative Block GroupExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Maximum postoperative pain intensity within 24 hours

The highest postoperative pain intensity measured using an 11-point numeric rating scale (NRS; 0 = no pain, 10 = worst pain imaginable) during the first 24 hours after surgery, assessed at 1, 6, 12, and 24 hours postoperatively.

Time frame
Within 24 hours after surgery

Secondary outcomes

1

Maximum postoperative pain intensity during post-anesthesia care unit stay

The highest postoperative pain intensity measured using an 11-point numeric rating scale (NRS; 0 = no pain, 10 = worst pain imaginable) during the recovery period.

Time frame
During the post-anesthesia care unit stay
2

Cumulative rescue opioid consumption within 24 hours

Total amount of rescue opioid administered between 1 and 24 hours after surgery.

Time frame
Within 24 hours after surgery
3

Incidence of postoperative nausea and vomiting

Occurrence of nausea or vomiting during the postoperative period.

Time frame
Within 24 hours after surgery

Other outcomes

Sponsors and contacts

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