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Phase 4 N=11 Treatment

Effect of Fosaprepitant on Motor Evoked and Somatosensory Evoked Potentials Under General Anesthesia

Postoperative Nausea

Enrolled (actual)
11
Serious AEs
0.0%
Results posted
Jul 2022
Primary outcome: Primary: Somatosensory Evoked Potentials (SEPs), Extremity Amplitude (Left Upper Extremity) — 2.685; 2.545; 2.58; 2.292 µV — p=0.35

Study Design & Population

Study type
Interventional
Phase
Phase 4
Interventions
Fosaprepitant 150 mg (Drug)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Stanford University
Primary completion
Jan 2020

Outcome Measures

OutcomeResultp-value
PRIMARY
Somatosensory Evoked Potentials (SEPs), Extremity Amplitude (Left Upper Extremity)
2.685; 2.545; 2.58; 2.292 0.35
PRIMARY
Somatosensory Evoked Potentials (SEPs), Extremity Amplitude (Right Upper Extremity)
2.38; 2.47; 2.27; 2.47 0.72
PRIMARY
Somatosensory Evoked Potentials (SEPs), Extremity Amplitude (Left Lower Extremity)
1.56; 1.56; 1.47; 1.35 0.93
PRIMARY
Somatosensory Evoked Potentials (SEPs), Extremity Amplitude (Right Lower Extremity)
1.7; 1.77; 1.81; 1.79 0.42
PRIMARY
Motor Evoked Potentials Amplitude (Left Upper Extremity)
1300; 1573.33; 1634.89; 1544.78 0.386

Summary

The purpose of this study is to determine if intravenous fosaprepitant can interfere with nervous system monitoring signals in patients having surgery under general anesthesia. This medication has numerous effects on the sensory nerve transmission which can theoretically have effects on the ability to accurately measure somatosensory evoked potentials.

Eligibility Criteria

Inclusion Criteria

  • Having a surgical procedure requiring general anesthesia, having a surgical procedure where neuromonitoing with somatosensory evoked potentials and motor evoked potentials neuromonitoring is requested by the surgical team

Exclusion Criteria

  • Patient refusal, allergy to the drug or any of its excipients, pre-operative motor or sensory deficit
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT03197064). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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