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Continuous Norepinephrine Administration and Blood Pressure Stability During Anesthetic Induction

U

Universitätsklinikum Hamburg-Eppendorf

Status

Completed

Conditions

Perioperative Hypotension
Blood Pressure

Treatments

Other: Continuous norepinephrine infusion via an infusion pump
Other: Manual bolus norepinephrine administration

Study type

Interventional

Funder types

Other

Identifiers

NCT05997303
2023-101053-BO-ff

Details and patient eligibility

About

This is a randomized trial investigating whether continuous norepinephrine administration via an infusion pump - compared to manual bolus administration - increases blood pressure stability within the first 15 minutes of anesthetic induction in non-cardiac surgery patients.

The secondary endpoints area under a MAP of 65, 60, 50, and 40 mmHg [mmHg × min], cumulative duration of a MAP <65, <60, <50, and <40 mmHg [min], area above a MAP of 100, 110, 120, and 140 mmHg [mmHg min], cumulative duration of a MAP >100, >110, >120, and >140 mmHg [min] and cumulative dose of norepinephrine indexed to body weight [μg/kg] within the first 15 minutes of anesthetic induction will be assessed.

Full description

not provided

Enrollment

72 patients

Sex

All

Ages

45+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • age ≥ 45 years
  • American Society of Anesthesiologists physical status II-IV
  • scheduled for elective major non-cardiac surgery under general anesthesia
  • continuous intraarterial blood pressure monitoring using a radial arterial catheter for clinical indications not related to the trial
  • sinus rhythm

Exclusion criteria

  • Clinical indication to use a continuous norepinephrine infusion via an infusion pump during anesthetic induction
  • Need for femoral artery catheterization
  • History of intracranial bleedings or aneurysms
  • Patients who are incapable of giving consent
  • Pregnancy

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

72 participants in 2 patient groups

Continuous norepinephrine administration
Other group
Description:
continuous norepinephrine infusion via an infusion pump; norepinephrine dose will be at the discretion of the treating anesthesiologists
Treatment:
Other: Continuous norepinephrine infusion via an infusion pump
Manual bolus norepinephrine administration
Other group
Description:
manual bolus norepinephrine administration; norepinephrine dose will be at the discretion of the treating anesthesiologists
Treatment:
Other: Manual bolus norepinephrine administration

Trial contacts and locations

1

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Central trial contact

Christina Vokuhl, M.D.

Data sourced from clinicaltrials.gov

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