Efficacy and Safety of Adding Dexmedetomidine to Levobupivacaine in Rectus Sheath Block Compared to Quadratus Lumborum Block in Patients Undergoing Lower Abdominal Cancer Surgery: A Randomized Clinical Trial

Trial statusNot yet recruiting
Trial phasePhase 4
Trial typeInterventional
Biological sexAll
Age18+
SponsorAssiut University

About this trial

Surgical trauma activates numerous receptors leading to severe postoperative pain. Seventy to seventy-five percent of the pain is somatic, originating from the anterior abdominal wall, and it often persists for 72 hours after open surgery. The objective of this study is to compare the efficacy and safety of adding dexmedetomidine to Levobupivacaine in rectus sheath block with quadrates lumborum block in patients undergoing lower abdominal cancer surgeries.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients subjected to major lower abdominal cancer surgeries.

The enrolled age will be from 18 years to 70 years

ASA I-III and NYHA I-III.

Disqualifiers

ASA physical status >III and NYHA>III

Patient refusal

Body mass index >40 kg/m2

Preoperative opioid consumption

Trial design

Design model

Parallel

Treatments tested in this trial

  • Levobupivacaine

    Drug

    40-ml mixture of 20 ml of 0.5% levobupivacaine diluted with 20 ml of 0.9% N.S. (20 ml to be injected on each side

  • Levobupivacaine + Dexmedetomidine

    Drug

    60 ml mixture of 1.5 mic/kg dexmedetomidine added to 30 ml of 0.5% levobupivacaine diluted with 30 ml of 0.9% N.S. (30 ml to be administered on each side, divided into 15 ml for the upper segment and 15 ml for the lower segment).

Treatment groups

122 Participants
are divided into 2 treatment groups
Group A: Quadratus lumborum block (QLB group)Experimental treatment 1 intervention
Group B: Rectus sheath block (RSB group)Experimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

pain intensity

measured by VAS immediately postoperatively, then at 2-, 4-, 6-, 8-, 12-, 18-, 24-hours after surgery.

Time frame
24 hours

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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