Comparison of Transversus Abdominis Plane and Erector Spinae Plane Blocks for Pain Control After Renal Laparoscopy

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-40
SponsorCairo University

About this trial

The goal of this study is to compare the analgesic efficacy of ultrasound-guided transversus abdominis plane (TAP) block versus erector spinae plane block (ESPB) in adult patients undergoing laparoscopic renal surgeries. Forty adults (18-60 years, ASA I-II) will be randomly assigned to receive either TAP or ESPB after induction of general anesthesia. Postoperative pain will be assessed using the Visual Analogue Scale (VAS) and total fentanyl consumption over 24 hours. Secondary outcomes include time to first analgesic request, hemodynamic parameters, patient satisfaction, and incidence of complications. The study will be conducted at Cairo University Hospitals following ethical approval, with all patients providing written informed consent.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age from 18 to 40 years old.

Both sexes.

American Society of Anesthesiology (ASA) physical status I, II.

Scheduled for laparoscopic renal surgeries under general anesthesia

Disqualifiers

Parent's refusal.

Coagulation disorders.

History of allergy to local anesthetics.

Infection or redness at the injection site.

Trial design

Design model

Parallel

Treatments tested in this trial

  • TAP Block

    Procedure/Surgery

    a bilateral ultrasound guided TAP block performed by injecting 20 ml of 0.25% bupivacaine into the TAP space after negative aspiration. a bilateral ultrasound guided ESP block performed by injecting 20 ml of 0.25% bupivacaine into the ESP space after negative aspiration.

Treatment groups

60 Participants
are divided into 2 treatment groups
Group A: TAP Block groupExperimental treatment 1 intervention
Group B: ESP Block groupExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Total fentanyl consumption.

Total fentanyl consumption in the first 24 hours (μg-microgram) postoperative.

Time frame
24 hours.

Secondary outcomes

1

Time to first rescue analgesia.

Time elapsed from the end of surgery until the patient requires the first dose of rescue analgesia.

Time frame
24 hours postoperatively.
2

Postoperative Pain scores.

pain assessment using Visual Analog Scale (VAS) score: pain level scored from 0 (no pain) to 10 (worst imaginable pain).

Time frame
At Post Anesthesia Care Unit (PACU) and 2,4,6,12,18,24 hours Postoperatively.
3

Hemodynamic Parameter Heart rate

Heart rate

Time frame
At PACU and 1,2,4,6,12,24 hours postoperatively.
4

Hemodynamic Parameter

mean arterial blood pressure

Time frame
At PACU and 1,2,4,6,12,24 hours postoperatively.

Other outcomes

Sponsors and contacts

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