Actively Recruiting

Phase Not Applicable
Age: 45Years +
All Genders
NCT07538388

Continuous Versus Bolus Norepinephrine Administration to Treat Postinduction Hypotension

Led by Universitätsklinikum Hamburg-Eppendorf · Updated on 2026-05-13

446

Participants Needed

4

Research Sites

29 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

INDUCT-Multi is a multicenter randomized trial investigating whether continuous, compared to bolus, administration of norepinephrine during induction of general anesthesia reduces postinduction hypotension in high-risk non-cardiac surgery patients.

CONDITIONS

Official Title

Continuous Versus Bolus Norepinephrine Administration to Treat Postinduction Hypotension

Who Can Participate

Age: 45Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients aged 45 years or older
  • Scheduled for elective major non-cardiac surgery under general anesthesia
  • Planned continuous intra-arterial blood pressure monitoring with a radial arterial catheter
  • At least two of the following risk factors for acute kidney injury: age 65 years or older, ASA physical status III or IV, chronic arterial hypertension, diabetes mellitus requiring medication, intra-abdominal surgery, preoperative renal insufficiency (serum creatinine 1.2 mg/dL)
Not Eligible

You will not qualify if you...

  • Pregnancy
  • Cardiac arrhythmia
  • History of intracranial hemorrhage or intracranial aneurysm
  • Clinical need for continuous norepinephrine infusion during anesthesia induction (e.g., severe aortic valve stenosis, coronary artery disease, or heart failure)
  • Unable to understand, read, and provide informed consent in German

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 4 locations

1

Department of Anesthesiology, University Hospital Duesseldorf, Heinrich Heine University Duesseldorf

Düsseldorf, Germany

Not Yet Recruiting

2

Department of Anaesthesiology, Intensive Care Medicine and Pain Medicine, University Hospital Giessen, Justus-Liebig University Giessen

Giessen, Germany

Not Yet Recruiting

3

Department of Anesthesiology, Center of Anesthesiology and Intensive Care Medicine, University Medical Center Hamburg-Eppendorf

Hamburg, Germany

Not Yet Recruiting

4

Department of Anaesthesiology, University Hospital LMU Munich

München, Germany

Actively Recruiting

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Research Team

K

Kristen K Thomsen, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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