Fact CheckerSign in

NCT06093971Completed

Remimazolam Versus Propofol for General Anesthesia Induction in Patients on Renin-angiotensin System Blockers Undergoing Robot-assisted Laparoscopic Prostatectomy

Remimazolam Versus Propofol for General Anesthesia Induction in Patients on Renin-angiotensin System Blockers Undergoing Robot-assisted Laparoscopic Prostatectomy: A Randomized Controlled Study

Source: ClinicalTrials.gov · Last updated 12 Dec 2024

Brief summary (registry, in English)

The investigators conduct a random assignment into either the remimazolam group or the propofol group. Depending on the group assignment, either remimazolam (0.2 mg/kg) or propofol (1.0 mg/kg) is administered. If necessary, additional doses of remimazolam (0.1 mg/kg) or propofol (0.5 mg/kg) are given. The standard anesthesia procedure of our institution is followed, and blood pressure data recorded during the surgery is analyzed (mean arterial pressure \<65mmHg is defined as hypotension).

Status (registry)
Completed
Study type
Interventional
Enrollment
112 (actual)
First submitted
12 Sept 2023
Start date
17 Nov 2023
Primary completion date
22 Oct 2024
Lead sponsor
Yonsei University
NCT number
NCT06093971

What you commit to

  • Study type: Interventional
  • Participants enrolled: 112
  • From 17 Nov 2023 to the primary completion date, 22 Oct 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • emergency surgery
  • Patients who did not take renin-angiotensin system blockers on the day of surgery

Lab values

  • Atrial fibrillation, moderate to severe valvular disease, ejection fraction of 35% or less

Other

  • If the subject includes those who cannot read the consent form (e.g. illiterate, foreigners, etc.)
  • cognitive dysfunction

Who the study is looking for

  • Patients who undergo robot-assisted laparoscopic prostatectomy and who have taken renin-angiotensin system blockers for more than 3 months.

Age in the registry: 19 years to - · Sex: Male · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Yonsei University College of Medicine
Coordinator of this site? Confirm its status
SeoulSouth KoreaUnknown status

Related publications

This page is information, not medical advice. Discuss any trial with your doctor.