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Clinical Trials/NL-OMON55117
NL-OMON55117RecruitingNot Applicable

The effect of proactive versus reactive treatment of hypotension on postoperative disability and outcome in surgical patients under anesthesia (PRETREAT): an adaptive, multicenter randomized controlled trial - PRETREAT

niversitair Medisch Centrum Utrecht0 sites5,000 target enrollmentStarted: TBDLast updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Sponsor
Enrollment
5,000

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional

Eligibility Criteria

Ages
18 to 99 (—)

Inclusion Criteria

  • Adult patients scheduled for elective non-cardiac surgery under general
  • anesthesia or central neuraxial anesthesia with a scheduled stay at the
  • hospital after surgery of at least one night - i.e. inpatients - will be
  • considered eligible for inclusion

Exclusion Criteria

  • Patients will be excluded when scheduled for low risk surgery, such as
  • ophthalmic surgery, endoscopic gastrointestinal procedures, and
  • (interventional) radiologic procedures. Also all other procedures under 30
  • minutes and obstetric or organ transplantations will be excluded.

Investigators

Sponsor
niversitair Medisch Centrum Utrecht

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