Clinical Trials Directory

Trials / Completed

CompletedNCT05103735

Propofol-remifentanyl Versus Dexmedetomidine in Awake Craniotomy: Impact on Electroclinical Seizure Activity

Propofol-remifentanil Versus Dexmedetomidine in Awake Craniotomy: an Intraoperative Neurophysiological Evaluation

Status
Completed
Phase
Study type
Observational
Enrollment
170 (actual)
Sponsor
Azienda Sanitaria-Universitaria Integrata di Udine · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Awake craniotomy require a cooperative patient during resection neurosurgery phase. Anesthesiologist should guarantee analgesia, sedation, nausea and vomiting prevention, while maintaining normal vital parameters. Neurosurgeon could be help by Intraoperative electrocorticography to maximise lesion resection and avoiding neurologic sequelae. Propofol and remifentanyl have been largely used. Dexmedetomidine represents an alternative. However little is known about the role of dexmedetomidine on Intraoperative electrocorticography.

Conditions

Interventions

TypeNameDescription
DRUGPropofolawake neurosurgery under propofol-remifentanil sedation

Timeline

Start date
2021-09-15
Primary completion
2021-10-10
Completion
2021-10-11
First posted
2021-11-02
Last updated
2023-01-31

Locations

1 site across 1 country: Italy

Source: ClinicalTrials.gov record NCT05103735. Inclusion in this directory is not an endorsement.