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Comparative Efficacity of Ephedrine Versus Norepinephrine to Correct Anesthesia Induction Related Hypotension

Comparison of Ephedrine Versus Norepinephrine Efficacity to Correct Anesthesia Induction Related Hypotension in Chronic Renal Insufficiency Patients

Status
UNKNOWN
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05497700
Enrollment
60
Registered
2022-08-11
Start date
2022-09-15
Completion date
2023-10-30
Last updated
2022-09-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hypotension on Induction

Brief summary

Hypotension occurs frequently after anesthesia induction and is more frequent in patients with chronic renal insufficiency. This hypotension occurs most frequently during the 20 minutes after anesthesia induction. Hypotension is commonly corrected by ephedrine bolus injection. However, presynaptic noradrenaline reserve may be lower in patients with chronic renal insufficiency rendering this treatment less effective. Another drug commonly used is norepinephrine, which action is independent of presynaptic noradrenaline storage. The primary hypothesis is that in patients with chronic renal insufficiency, bolus injection of norepinephrine will be more effective then ephedrine injections to correct hypotension after anesthesia induction. 60 patients with a glomerular filtration rate less than 45 mL/min/m2 (KDIGO classification less than grade 3b) will be included in this prospective double blind trial. All patients will be anesthetized by target-controlled infusion of propofol adjusted to a patient state index (Measured by Sedline, Masimo) of 25-50. Sufentanil injection will be based on noxious stimuli according to the attending anesthesiologist's judgement. Non-invasive blood pressure will be measured at the pre-anesthesia clinic, before induction and every minute up to 20 minutes post anesthesia induction. Episodes of hypotension, defined as a mean arterial blood pressure less than 65 mm Hg, will be treated either by a bolus injection of 6 mg ephedrine or a bolus injection of 6 mcg norepinephrine, which are equipotent doses. Seringues containing either ephedrine 3 mg/mL or norepinephrine 3 mcg/mL will be prepared by an anesthesia nurse not involved in the care of the patient and labeled as VASO-IRC-inclusion number. Randomization will be done by a computer generated list in a block randomization of 5. Primary outcome is the number of boluses needed to maintain arterial blood pressure above a mean of 65 mm Hg.

Interventions

DRUGEphedrine

Bolus injection of 6 mg ephedrine to keep mean arterial blood pressure above 65 mm Hg

DRUGNorepinephrine

Bolus injection of either 6 mcg norepinephrine to keep mean arterial blood pressure above 65 mm Hg

Sponsors

Brugmann University Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Masking description

Drug will be prepared by an anesthesia nurse not involved in the care of the patient and labeled as VASO-IRC-inclusion number.

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* elective non-cardiac surgery * general anesthesia * chronic renal insufficiency defined as a glomerular filtration rate \< 45 mL/min/m2

Exclusion criteria

* cardiac insufficiency with a left ventricular ejection fraction \< 50% * severe cardiomyopathy * severe cardiac valvular disease * use of enzyme converting inhibitors or sartans less than 24h before surgery * use of alpha2 antihypertension medication * chronic treatment by: noradrenaline or dopamine recapture inhibitors, tricyclic antidepressants, monoamine oxidase inhibitors

Design outcomes

Primary

MeasureTime frameDescription
Number of boluses20 minutes after anesthesia inductionPrimary outcome is the number of boluses of either ephedrine or norepinephrine needed to keep mean arterial blood pressure above 65 mm Hg

Countries

Belgium

Contacts

Primary ContactDenis Schmartz, MD
denis.schmartz@chu-brugmann.be+3224773996
Backup ContactZakaria Cheffi, MD
Zakaria.CHEFFI@chu-brugmann.be+3224773996

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026