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Therapeutic Study Evaluating the Efficacy of Noradrenaline in the Prevention of Hypotension Related to Intubation for Cardiac or Thoracic Surgery

Phase 3 Therapeutic Interventional Study Evaluating the Efficacy of Noradrenaline in the Prevention of Hypotension Related to Intubation for Cardiac or Thoracic Surgery - Single-centre Prospective Randomised Controlled Study With Blinded Assessment of the Primary Endpoint

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05335954
Acronym
EPITUBE-HEART
Enrollment
211
Registered
2022-04-20
Start date
2022-04-27
Completion date
2023-12-12
Last updated
2024-03-07

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

Conditions

Cardiac Disorder, Hypotension

Keywords

general anesthesia, intubation, cardiac surgery, hypotension, noradrenaline

Brief summary

Arterial hypotension during general anaesthesia (GA) is a serious event. While hypotension can occur during surgery, it usually occurs following induction of GA (i.e. following the injection of drugs to enable intubation). This is due to the injection of large doses of anaesthetic drugs with a vasodilatory effect over a short period of time to induce a deep sleep to allow intubation to take place for artificial ventilation. The prevention of hypotension during surgery has been extensively studied. In contrast, the prevention of hypotension following GA induction has been the subject of only two randomised studies in the ICU and three non-randomised studies in the OR with small numbers of patients. The level of evidence for the use of noradrenaline in the operating theatre remains low. The hypothesis of the study is that noradrenaline initiated during preoxygenation can reduce the incidence of hypotension during induction of general anaesthesia.

Interventions

noradrenaline

Sponsors

Nantes University Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
DOUBLE (Subject, Outcomes Assessor)

Masking description

Patient under anesthesia will not be aware of randomisation arm. the team collecting primary endpoint (hypotension under 55 mg during the 20 minutes after the start of anesthesia) will not be aware of patient assignation.

Eligibility

Sex/Gender
ALL
Age
18 Years to 90 Years
Healthy volunteers
No

Inclusion criteria

* Requiring cardiac or thoracic surgery under general anaesthesia * Requiring a blood pressure catheter prior to GA induction

Exclusion criteria

* Hemodynamic instability on arrival in the operating room * Hypotension on arrival in the operating theatre: Systolic blood pressure \< 100 mmHg or Mean arterial pressure \< 65 mmHg * Hypertension on arrival at the operating theatre: Systolic blood pressure \> 160 mmHg or Mean arterial pressure \> 100 mmHg * Adult under guardianship, curatorship or safeguard of justice * Unable to give consent * Pregnant or breastfeeding woman * Emergency surgery (cannot be delayed by 24 hours) * Current participation in an interventional protocol that interferes with the evaluation criteria of the study * Not affiliated to or not benefiting from a social security scheme * Lack of informed and written consent from the patient * Patient with a dilated aorta with a risk of rupture (e.g. chronic dissection for example) * Patient with severe aortic insufficiency * Treated hypertensive history that may have hypersensitivity to noradrenaline and hypertensive flares hypertensive attacks

Design outcomes

Primary

MeasureTime frameDescription
Intubation-related hypotensionWithin 20 minutes of the start of general anesthesia (induction)Occurrence of at least one episode of arterial hypotension defined by a Mean Arterial Pressure below 55 mmHg with Mean Blood Pressure = (Systolic Blood pressure + 2xDiastolic Blood Pressure)/3

Secondary

MeasureTime frameDescription
Occurrence of complicationsWithin 20 minutes of the start of the intubationOccurrence (yes/no) of complications related to the intubation: Desaturation \< 80%, Severe hypotension (defined as hypotension with systolic blood pressure \< 80mmHg), Cardiac arrest, Death during intubation, Difficult intubation (more than two laryngoscopies and/or the use of an alternative technique after optimization of head position, with or without external laryngeal manipulation), Heart rhythm disorder (ventricular extrasystole, ventricular fibrillation, ventricular tachycardia) Esophageal intubation, Regurgitation/inhalation, Tooth breakage
Total dose of vasopressorWithin 20 minutes of the start of the intubationTotal dose of vasopressors (noradrenaline, ephedrine, neosynephrine)
Duration of episodes of hypotensionWithin 20 minutes of the start of the intubationCumulative duration of episodes of hypotension \< 55mmHg
Hypotension eventWithin 20 minutes of the start of the intubationAt least one Mean Arterial Pressure measurement \< 65 mmHg
Hypertension eventWithin 20 minutes of the start of the intubationAt least one Systolic Blood Pressure measurement \> 160 mmHg or Mean Arterial Pressure \> 100mmHg
ECC Cardiac OutputWithin 20 minutes of the start of the intubationExtra Corporeal Circulation generated Cardiac Output frequency in bpm (beat per minute)
ECC Arterial Line PressureWithin 20 minutes of the start of the intubationExtra Corporeal Circulation generated Arterial Line Pressure in mmHg
ECC Arterial Line TemperatureWithin 20 minutes of the start of the intubationExtra Corporeal Circulation generated Arterial Line Temperature in degree Celcius
ECC Mean Arterial PressureWithin 20 minutes of the start of the intubationExtra Corporeal Circulation generated Mean Arterial Pressure in mmHg
ECC VO2Within 20 minutes of the start of the intubationExtra Corporeal Circulation generated VO2 (Volume O2) in Liter per Minute
ECC SaO2Within 20 minutes of the start of the intubationExtra Corporeal Circulation generated SaO2 (Arterial Saturation in O2) in percentage
ECC SvO2Within 20 minutes of the start of the intubationExtra Corporeal Circulation generated SvO2 (Venous Saturation in O2) in percentage
ECC durationWithin 20 minutes of the start of the intubationExtra Corporeal Circulation duration in minutes
ECC PaCO2Within 20 minutes of the start of the intubationExtra Corporeal Circulation generated PaCO2 (Arterial Pressure in CO2) in kPa
Delirium scoreAfter extubation within 48 hours postoperativelyAt least episode with ICDSC (Intensive Care Delirium Screening Checklist) score of 4 or more (0 to 8, binary interpretation with scores from 0 to 4 excluding the presence of delirium and scores greater than or equal to 4 indicating the presence of delirium, the highest scores are not related with greater intensity of delirium)
Duration of Noradrenaline and Dobutamine treatmentsWithin 28 days after surgeryDuration of treatment with Noradrenaline (in hours) and Dobutamine (in hours)
PaO2/FiO2In the 5 post-operative daysLowest value of PaO2/FiO2 (Arterial Pressure of O2 / Fraction inspired in Oxygen) measured
DialysisWithin 28 days after surgeryUse of dialysis in intensive care (Yes/No)
Hemolysis indexIn the 5 post-operative daysMaximum hemolysis index (0 to 10000, with higher scores being more pejorative)
Acute renal failureIn the 5 post-operative daysOccurrence of acute renal failure. This criterion will be assessed using the KDIGO (Kidney Disease: Improving Global Outcomes) scale (stage 1 to 3 with higher stages being more pejorative). Any renal attack defined as at least stage I according to this classification (1.5 to 1.9 times the base rate) will be considered as acute renal failure. The urinary output assessment component of the KDIGO scale will not be used because of the frequency of use of diuretics in cardiac surgery.
CVAIn the 5 post-operative daysOccurrence of a CVA (cerebrovascular accident)
Postoperative invasive ventilation durationUntil 28 days after surgeryDuration of postoperative invasive ventilation in hours: this duration is defined by the duration of mechanical ventilation between arrival in intensive care and extubation
Stay in intensive care durationUntil 28 days after surgeryLength of stay in intensive care in days: this duration is evaluated between the day of arrival in intensive care and the date on which the patient is considered to have left intensive care (no longer subject to monitoring in intensive care).
Hospitalization durationUntil 28 days after surgeryLength of hospitalization in days
MortalityUntil 28 days after surgeryDeath of the patient
ECC PaO2Within 20 minutes of the start of the intubationExtra Corporeal Circulation generated PaO2 (Arterial Pressure in O2) in kPa

Countries

France

Outcome results

None listed

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