Skip to content

Two Doses of Dexmedetomidine as Adjuvent to Bupivacaine in Tap Block

Comparing the Analgesic Effect of Two Different Doses of Dexmedetomidine Added to Bupivacaine in Ultrasound-guided Transversus Abdominis Plane Block in Patients Undergoing Lower Abdominal Cancer Surgeries; A Randomized Clinical Trial

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06624319
Acronym
Dexmed/tap
Enrollment
50
Registered
2024-10-02
Start date
2025-01-31
Completion date
2026-02-28
Last updated
2024-10-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Post Operative Pain

Keywords

Tap block, Dexmedetomidine

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.

Interventions

DRUGDexmedetomidine as adjuvent to bupvacaine in tap block

The analgesic effect of Two different doses of dexmedetomidine as adjuvent to bupivacaine in tap block

Sponsors

Assiut University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

Patients will receive pre-emptive ultrasound-guided tap block with two different doses of 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.

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Total morphine consumption during the first 24 hours postoperativelyFirst 24 hours postoperativeMorphine consumption during the First 24 hours postoperative

Secondary

MeasureTime frameDescription
Severity of pain using Visual analogue scaleFirst 24 hours postoperativeThe 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 postoperativeusing 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)

Countries

Egypt

Contacts

Primary ContactKerolos S Tawfeek, Resident
Kerolossalama7@gmail.com+2001551990411
Backup ContactMohanad A Mohamed
Mohanad.abosagheer@gmail.com+2001027068866

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026