drugset / Trial / NCT03311581
The Feasibility of Propofol TCI in Hemodialysis Patients Undergoing Arteriovenous Shunt Surgery
RandomizedParallel-groupSingle-blindTreatment
Summary
Written informed consent must be obtained before any study specific procedures are undertaken. Informed consent will be obtained during pre-operative assessment.
Timeline
- Start
- 2017-09-11
- Primary completion
- 2021-06-04
- Completion
- 2021-06-04
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Propofol | Small molecule | — | — |
| Subject | Sevoflurane | Other / unclassified | — | Inhaled |