Clinical Trials Directory

Trials / Completed

CompletedNCT03236727

SSEP Fluctuations Due to Dexmedetomidine During Posterior Spine Fusion

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
25 (actual)
Sponsor
George Papanicolaou Hospital · Academic / Other
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

Intravenous anesthetic agents as far as inhaled agents produce a dose depended increase in latency and decrease in amplitude of SomatoSensory Evoked Potential (SSEP). Dexmetedomidine, a highly selective a2 adrenergic agonist, not only minimizes the anesthetic agents but also the opioids, reducing the analgesic demands. The effect of dexmedetomidine on SSEP has not been elucidated. We aimed to investigate alterations on somatosensory SSEP in adults during posterior spinal fusion surgery before and after Dexmedetomidine administration.

Detailed description

Patients 18-75 years old, ASA (physical status classification system) I-III, scheduled for elective posterior spinal fusion surgery were enrolled in this prospective study. After induction in anesthesia, it was applied SSEP monitoring and a baseline test was performed after 15min (in order to wash out the propofol used for induction). Infusion of Dexmedetomidine was started at a bolus dose of 1mcg/Kg following by 0.7mcg/Kg. Bispectral Index (BIS) monitored the depth of anesthesia and an adequate level (40-50) of anesthesia was maintained by sevoflurane. SSEP were recorded intraoperatively from the tibial nerve (P37) and data were analyzed over that period.

Conditions

Interventions

TypeNameDescription
DRUGDexmedetomidineChanges of both amplitude and latency of SSEPs during dexmedetomidine infusion.

Timeline

Start date
2014-03-01
Primary completion
2016-05-01
Completion
2016-06-01
First posted
2017-08-02
Last updated
2017-08-03

Source: ClinicalTrials.gov record NCT03236727. Inclusion in this directory is not an endorsement.