Clinical Trials Directory

Trials / Completed

CompletedNCT02089932

Dexmedetomidine in Different Dose Levels as Adjuvant to Bupivacaine-induced Ultrasound-guided Femoral Nerve Block.

The Effects of Different Dose Levels of Peri-neural Dexmedetomidine on the Pharmacodynamic and Side Effects Profiles of Bupivacaine-induced Ultrasound-guided Femoral Nerve Block

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
60 (actual)
Sponsor
Cairo University · Academic / Other
Sex
All
Age
15 Years – 45 Years
Healthy volunteers
Not accepted

Summary

The duration of sensory block after single dose of long acting local anesthetics is not sufficient to avoid the postoperative use of opioids. Alpha-2 adrenoceptor agonists such as clonidine have been shown to increase the duration of peripheral nerve block. Dexmedetomidine is a more potent and selective α-2-adrenoceptor compared to clonidine. To the best of our knowledge, the use of Dexmedetomidine in different dose levels as adjuvant to local anesthetic was not previously reported for femoral nerve block.

Conditions

Interventions

TypeNameDescription
DRUGperi-neural dexmedetomidine as adjuvant to bupivacaine in femoral nerve blockultrasound guided femoral nerve block with injection of 25 ml bupivacaine 0.5% perineurally with 1 ml dexmedetomidine 25, 50, or 75 microgram perineurally. After adequate assessment of femoral nerve block, patients will be transferred to the operating room to receive a standard general anesthesia.
DRUGPlacebo

Timeline

Start date
2014-02-01
Primary completion
2015-04-01
Completion
2015-06-01
First posted
2014-03-18
Last updated
2019-01-15

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT02089932. Inclusion in this directory is not an endorsement.