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2025-521784-12-00RecruitingPhase 4

Remimazolam versus propofol for deep sedation during Endoscopic Ultrasound (EUS) procedures. A randomized controlled trial.

Source: EU CTIS (euclinicaltrials.eu) · Last updated 10 Sept 2026

Next steps

Brief summary (registry, in English)

To compare a remimazolam-based sedation regimen managed by endoscopists to a propofol-based sedation regimen performed by anesthesiologists during EUS gastrointestinal procedures.

Status (registry)
Recruiting
Phase (registry)
Phase 4
Study type
Interventional
Enrollment
332 (estimated)
First submitted
25 Jul 2025
Start date
23 Jun 2026
Lead sponsor
Ospedale San Raffaele S.r.l.
EU CT number
2025-521784-12-00

What you commit to

  • Study type: Interventional · Phase 4
  • Planned participants: 332
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of EU CTIS (euclinicaltrials.eu). It describes the study design.

AI-kivonat: who the study is looking for

Machine-read from the registry text on this page, so it can be wrong. The registry text below and the trial team decide who can take part.

The trial is looking for adults who are booked for a planned endoscopic ultrasound of the digestive tract as outpatients. It compares two ways of giving deep sedation.

Age
Over 18 years
Sex
All sexes can join

Main reasons for not taking part

  • Urgent endoscopic ultrasound procedures
  • Known reasons why propofol or remimazolam cannot be used
  • Procedures that need a breathing tube through the mouth
  • Pregnant or breastfeeding women
  • Inpatient procedures

Read by machine on 9 Nov 2026.

Who cannot take part

Copied verbatim from EU CTIS (euclinicaltrials.eu) and grouped by topic. Only the trial team decides who can take part.

Age

  • Patients < 18 years

Other

  • Patients scheduled for urgent EUS gastrointestinal procedures
  • Known contraindications to the use of propofol and/or remimazolam
  • Patient’s refusal to participate
  • Procedures that require orotracheal intubation
  • Pregnant and breastfeeding women
  • Inpatient procedures

Who the study is looking for

  • Patients >18 years
  • Patients scheduled for elective EUS gastrointestinal procedures
  • Signed informed consent
  • Outpatient procedures

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on EU CTIS (euclinicaltrials.eu)

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Ospedale San Raffaele S.r.l.MilanItalyRecruiting

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