NCT03465423View on ClinicalTrials.gov

Comparison of Propofol Requirement Between Patients With Pituitary Somatotroph Tumor and With Nonfunctioning Pituitary Tumor in Transsphenoidal Pituitary Surgery Under Total Intravenous Anesthesia

CompletedOBSERVATIONAL
Enrollment

62

Participants

Timeline

Start Date

March 20, 2018

Primary Completion Date

December 4, 2018

Study Completion Date

December 4, 2018

Conditions
Pituitary Tumor
Interventions
PROCEDURE

Not applicable (measuring subject's effect site concentration of propofol during the induction of general anesthesia)

The patients of two cohort group will undergo general anesthesia in the same way and therefore there is no intervention in this study.

Trial Locations (1)

120-752

Associate Professor Department of Anesthesiology and Pain Medicine, Seoul

All Listed Sponsors
lead

Yonsei University

OTHER

NCT03465423 - Comparison of Propofol Requirement Between Patients With Pituitary Somatotroph Tumor and With Nonfunctioning Pituitary Tumor in Transsphenoidal Pituitary Surgery Under Total Intravenous Anesthesia | Biotech Hunter | Biotech Hunter