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Techniques for Perioperative Analgesia for Live Liver Donors; A Pilot Study

A

Ain Shams University

Status and phase

Unknown
Phase 4

Conditions

Anesthesia

Treatments

Drug: Dexmedetomidine
Procedure: Ultrasound guided TAP block
Drug: Fentanyl infusion

Study type

Interventional

Funder types

Other

Identifiers

NCT03393988
FMASU R45/2017

Details and patient eligibility

About

This study,will evaluate the efficacy of ultrasound (US)-guided subcostal oblique TAP block together with IV infusion of Dexmedetomidine and fentanyl as a type of multimodal analgesic regimen in comparison with IV fentanyl based analgesia only in live liver donors.

Enrollment

20 patients

Sex

All

Ages

20 to 50 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • American Society of Anesthesia (ASA) physical status I or II
  • Scheduled as live liver donors
  • J-shaped incision in the supraumblical region

Exclusion criteria

  • Patients with a history of psychiatric/neurological illness,
  • Hypertensive patients,
  • Morbidly obese patients,
  • Pregnant and nursing women,
  • Patients with known allergic reaction to any of the study medications,
  • Patients on recent use of sedatives or analgesics,
  • Patients with significant laboratory abnormalities

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

20 participants in 2 patient groups

Group F
Active Comparator group
Description:
Fentanyl infusion (0.5 µg/kg/hr)
Treatment:
Drug: Fentanyl infusion
Group (TAP-Dex)
Active Comparator group
Description:
Ultrasound guided TAP block and Dexmedetomidine * Ultrasound guided subcostal oblique TAP block with 0.25 % bupivacaine * Dexmedetomidine infusion(200 µg in 2 ml diluted in 48 ml of saline) * Fentanyl infusion (0.5 µg/kg/hr).
Treatment:
Drug: Fentanyl infusion
Procedure: Ultrasound guided TAP block
Drug: Dexmedetomidine

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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