Combined Subcostal and Lateral Transversus Abdominis Plane Block for Postoperative Analgesia Versus Thoracic Epidural Analgesia in Patients Undergoing Major Abdominal Cancer Surgery

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorAssiut University

About this trial

This study aims to evaluate the safety and efficacy of combined subcostal and lateral transversus abdominis plane (TAP) for postoperative analgesia versus thoracic epidural anesthesia (TEA) in patients undergoing major abdominal cancer surgery.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age ≥ 18 years.

Both sexes.

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

Scheduled for major abdominal surgeries including: (e.g., gastrectomy, colectomy, hepatectomy, cystectomy, total abdominal hysterectomy, Nephrectomy, pancreatectomy).

Disqualifiers

Intraoperative hemodynamic instability.

History or evidence of coagulopathy.

Infection or abdominal wall masses at injection site.

Morbid obesity.

Trial design

Design model

Parallel

Treatments tested in this trial

  • Subcostal and lateral transversus abdominis plane block

    Other intervention

    Patients will receive an ultrasound-guided combined subcostal and lateral transversus abdominis plane block.

  • Thoracic epidural anesthesia

    Other intervention

    Patients will receive an ultrasound-guided thoracic epidural anesthesia.

Treatment groups

50 Participants
are divided into 2 treatment groups
Group A: Subcostal and lateral transversus abdominis plane block groupExperimental treatment 1 intervention
Group B: Thoracic epidural anesthesia groupActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Total morphine consumption

Rescue analgesia of morphine will be given as 3 mg bolus if the Visual Analogue Scale (VAS) \> 3 to be repeated after 30 min if pain persists until the VAS \< 4.

Time frame
24 hours postoperatively

Secondary outcomes

1

Time to the 1st rescue analgesia

Time to the first request for the rescue analgesia (time from the end of surgery to first dose of morphine administrated).

Time frame
24 hours postoperatively
2

Mean arterial pressure

Mean arterial pressure will be recorded before skin incision, one minute after skin incision and then recorded regularly every 10 minutes.

Time frame
Till the end of surgery (Up to 2 hours)
3

Heart rate

Heart rate will be recorded before skin incision, one minute after skin incision and then recorded regularly every 10 minutes.

Time frame
Till the end of surgery (Up to 2 hours)
4

Degree of pain

Each patient will be instructed about postoperative pain assessment with the Visual Analogue Scale (VAS). VAS (0 represents "no pain" while 10 represents "the worst pain imaginable"). VAS will be assessed at 0, 4, 6, 8, 12, and 24 h postoperatively.

Time frame
24 hours postoperatively

Other outcomes

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