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SSEP Fluctuations Due to Dexmedetomidine During Posterior Spine Fusion

SSEP Fluctuations Due to Dexmedetomidine During Posterior Spine Fusion

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03236727
Enrollment
25
Registered
2017-08-02
Start date
2014-03-31
Completion date
2016-06-30
Last updated
2017-08-03

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

Conditions

Spinal Fusion

Keywords

Dexmedetomidine, spinal fusion, SSEP

Brief 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.

Interventions

DRUGDexmedetomidine

Changes of both amplitude and latency of SSEPs during dexmedetomidine infusion.

Sponsors

George Papanicolaou Hospital
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* Patients with ASA physical status 1-3

Exclusion criteria

* Patients with ASA physical status \>3, * Body Mass Index (BMI) over 30, * indication for rapid sequence induction, * any contraindication for receiving b-blocker, * Glasgow Coma Scale (GCS) \<13, * history of drug abuse, * neurologic deficit or preoperatively foreseen delayed extubation, * preoperative heart rate\<45.

Design outcomes

Primary

MeasureTime frameDescription
SSEPs10 min after starting infusion of dexmedetomidinemeasurement of SSEPs parameters regarding the baseline.

Outcome results

None listed

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