About this trial
This study intends to measure the ED95 of remimazolam-assisted sedation in arteriovenous fistula creation by BCD.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
18-65 years old (including borderline values).
Elective surgical patients under local anaesthesia for operation of AVF
Voluntary participation in this study and signing of informed consent.
American Society of Anesthesiologists (ASA) classification < Grade IV.
Disqualifiers
hypersensitivity to remimazolam or benzodiazepines.
patients with severe cardiac, pulmonary, neurological diseases or liver failure. -- Preoperative use of sedative drugs, anticonvulsants, etc.
patients who cannot cooperate with postoperative recovery or follow-up.
vulnerable groups, including those with mental illness, cognitive impairment, critically ill patients, pregnant women, illiterates, etc.
Trial design
Single group
Treatments tested in this trial
remimazolam sedation
Drugremimazolam sedation
Treatment groups
Trial outcomes
Primary outcomes
ED95
the dose of Remimazolam that provides satisfactory sedation in 95% of patients.
Locations
Sponsors and contacts
Click on the lead sponsor to view all of their trials.
Gang Chen
Lead sponsor
Sir Run Run Shaw Hospital
Sponsor institution
This trial is not recruiting at the moment. You can still explore other options: