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Oscillometric Versus Intraarterial Blood Pressure Monitoring During Robot-Assisted Prostatectomy (PROST-BP)

U

University of Hamburg-Eppendorf

Status

Enrolling

Conditions

Intraoperative Hypotension

Treatments

Other: Oscillometric blood pressure monitoring
Other: Intraarterial blood pressure monitoring

Study type

Interventional

Funder types

Other

Identifiers

NCT07349186
2025-101598-BOff

Details and patient eligibility

About

The PROST-BP trial is a prospective, single-center, randomized, patient-blinded, non-inferiority trial investigating whether intermittent oscillometric blood pressure monitoring is non-inferior to continuous intraarterial blood pressure monitoring in reducing intraoperative hypotension in patients having robot-assisted radical prostatectomy.

Enrollment

210 estimated patients

Sex

Male

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • male patient ≥18 years
  • scheduled for elective robot-assisted (Da Vinci) radical prostatectomy in steep Trendelenburg position
  • planned intraarterial blood pressure monitoring

Exclusion criteria

  • patients in whom the attending anesthesiologist considers intraarterial blood pressure monitoring to be mandatory for clinical reasons
  • patients participating in another interventional trial likely to influence intraoperative blood pressure management

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

210 participants in 2 patient groups

Oscillometric blood pressure monitoring
Experimental group
Description:
Intraoperative blood pressure will be managed based on oscillometric blood pressure monitoring.
Treatment:
Other: Oscillometric blood pressure monitoring
Intraarterial blood pressure monitoring
Active Comparator group
Description:
Intraoperative blood pressure will be managed based on intraarterial blood pressure monitoring.
Treatment:
Other: Intraarterial blood pressure monitoring

Trial contacts and locations

1

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Central trial contact

Alina Bergholz; Bernd Saugel

Data sourced from clinicaltrials.gov

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