Effects of Sufentanil on the Intraoperative Hemodynamics
ConditionIntraoperative Hypotension
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age19+
SponsorSeoul National University Hospital
About this trial
This study is a randomized, controlled trial. A total of 92 patients will be randomized to receive sufentanil or remifentanil during extracranial-intracranial bypass surgery.
Eligibility criteria
Qualifiers
Patients who undergo elective extracranial-intracranial bypass surgery
American Society of Anesthesiologists grade 1,2,3
Age > 18 years old
Disqualifiers
Refuse to participate to the study
American Society of Anesthesiologists grade 4
Body Mass Index < 18.5 kg/m2 or > 35 kg/m2
Allergic history of opioid
Trial design
Treatments tested in this trial
- Sufentanil
- Remifentanil
Treatment groups
92 Participants
are divided into 2 treatment groupsSponsors and collaborators
Source ClinicalTrials.gov