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Comparison between Remimazolam and Propofol in patients undergoing Monitored Anesthesia Care for Peripheral Angioplasty: a randomized controlled trial

Comparison between Remimazolam and Propofol in patients undergoing Monitored Anesthesia Care for Peripheral Angioplasty: a randomized controlled trial - Remimazolam anesthesia for peripheral angioplasty

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000057411
Enrollment
88
Registered
2025-04-07
Start date
2025-04-07
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Monitored Anesthesia Care for Peripheral Angioplasty

Interventions

In the intervention group, monitored anesthesia care is performed using intravenous remimazolam infusion. In the intervention group, monitored anesthesia care is performed using intravenous propofol i

Sponsors

Seoul National University Bundang Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: - ASA I-III - Patients with peripheral vascular disease - Peripheral angioplasty under monitored anesthesia care

Exclusion criteria

Exclusion criteria: - ASA IV, V - Pregnancy - Preexisting renal or hepatic dysfunction - Patients with heart failure (EF <40%) - Patients with coronary artery disease planning for interventional or surgical treatment - Patient contraindicated for propofol or remimazolam administration (e.g. anaphylaxis) - Alcohol or drug abuse - Glaucoma - Sleep apnea

Design outcomes

Primary

MeasureTime frame
Total phenylephrine dose require to restore blood pressure during hypotensive events during the procedure

Secondary

MeasureTime frame
- The number of hypotension events - Intraoperative vital signs: blood pressure, heart rate, pulse oximeter - Recovery room stay time - Patient satisfaction - Surgeon satisfaction - Adverse effects: arrhythmia, respiratory depression, anesthetic method conversion, unplanned ICU admission, intraoperative/postoperative nausea and vomiting) - PPostoperative analgesic requirement

Countries

Asia(except Japan)

Contacts

Public ContactJin-Woo Park

Seoul National University Bundang Hospital Department of Anesthesiology and Pain Medicine

jinul8282@gmail.com82-31-787-7499

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026