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Two Doses of Dexmedetomidine as Adjuvent to Bupivacaine in Tap Block

Not Applicable
Not yet recruiting
Conditions
Post Operative Pain
Interventions
Registration Number
NCT06624319
Lead Sponsor
Assiut University
Brief Summary

The aim of this study to determine the optimal dose of dexmedetomidine as an adjuvant to bupivacaine in U.S guided TAP block for preemptive analgesia In patients undergoing lower abdominal cancer surgeries.

Detailed Description

The transversus abdominis plane (TAP) involves innervations of the anterolateral abdominal wall derived from T6-L1. The block can be given either by anatomical landmark technique or by using an ultrasound probe. The local anesthetic is deposited in a plane between internal oblique and transversus abdominis muscle. It provides adequate postoperative analgesia following various abdominal surgeries.Dexmedetomidine is an alpha-2 agonist that has been approved as a venous sedative and an adjuvant for pain relief .In previous studies, the addition of dexmedetomidine to bupivacaine in the TAP block has prolonged the effect of this block . So far, the optimal dose of dexmedetomidine for the TAP block has not been determined.

Recruitment & Eligibility

Status
NOT_YET_RECRUITING
Sex
All
Target Recruitment
50
Inclusion Criteria
  • age from 18 to 65 years old
  • lower abdominal cancer surgery
Exclusion Criteria
  • patient refusal
  • the local anesthetic allergy
  • coagulopathy
  • local infection at the procedure site
  • psychic patients
  • patient on chronic opioid use

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
tap block with 0.5 μg/kg dexmedetomidineDexmedetomidine as adjuvent to bupvacaine in tap blockwill receive pre-emptive ultrasound-guided tap block with 0.5 μg/kg dexmedetomidine in 20 ml volume added to 20 mL of 0.25% bupivacaine (40 ml in total) 20 ml will be applied on each side of the abdominal wall after induction of GA.
tap block with 1.5 μg/kg dexmedetomidineDexmedetomidine as adjuvent to bupvacaine in tap blockwill receive pre-emptive ultrasound-guided tap block with 1.5 μg/kg dexmedetomidine in 20 ml volume added to 20 mL of 0.25% bupivacaine (40 ml in total) 20 ml will be applied on each side of the abdominal wall after induction of GA.
Primary Outcome Measures
NameTimeMethod
Total morphine consumption during the first 24 hours postoperativelyFirst 24 hours postoperative

Morphine consumption during the First 24 hours postoperative

Secondary Outcome Measures
NameTimeMethod
Severity of pain using Visual analogue scaleFirst 24 hours postoperative

The severity of pain at rest and on coughing will be assesd using a 10-cm vas(0 means no pain ,10 means worst pain)

Patient level of sedation using four point modified ramsy scaleFirst 24 hours postoperative

using a 4-point scale (0 = awake and alert, 1 = minimally sedated, responds to speech, 2 = moderately sedated, arousable by tactile stimulation, and 3 = deeply sedated, arousable only by painful stimulation)

Trial Locations

Locations (1)

South egypt cancer institute,Assiut University

🇪🇬

Assiut, Egypt

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