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Individualized Blood Pressure Management in Patients Undergoing Cardiac Surgery (PRECISE)

20. november 2019 opdateret af: Meshalkin Research Institute of Pathology of Circulation

Individualized Blood Pressure Management in Patients Undergoing Cardiac Surgery. A Pilot, Randomized Controlled Study

This pilot randomized-controlled study will determine the feasibility of large study comparing individualized versus standard blood pressure (BP) management in patients undergoing cardiac surgery under cardiopulmonary bypass (CPB). Our hypothesis is that maintaining higher BP levels based on preoperative measurements will reduce the incidence of major complications (composite outcome).

Studieoversigt

Status

Trukket tilbage

Betingelser

Intervention / Behandling

Detaljeret beskrivelse

Adequate hemodynamic control is a cornerstone in management in patients undergoing different types of surgery. Among all perioperative risk factors, the association between perioperative hypotension and adverse clinical outcomes in noncardiac and cardiac surgery patients is well defined.

Numerous factors are responsible for development of perioperative hypotension. They include but not limited to perioperative use of renin-angiotensin-aldosterone system and calcium channel blockers, hypovolemia, hemodilution, bleeding and inflammatory response syndrome.

To date, several evidence has been accumulated indicating that intraoperational hypertension can be hazardous.

It was shown that even short durations (1 to 5 min) of an intraoperative mean arterial pressure < 55 mmHg were associated with myocardial injuries and acute kidney injury (AKI).

Results of recent large retrospective cohort study conducted in adult patients who underwent cardiac surgery requiring CPB showed that postoperative stroke was strongly associated with sustained mean arterial pressure of less than 64 mmHg during cardiopulmonary bypass.

In patients undergoing CABG the overall incidence of combined cardiac and neurologic complications was significantly lower in the group where MAP during CPB was relatively high (80-110 mmHg) than in the low pressure group (MAP 50-60 mmHg) (p = 0.026). For each of the individual outcomes the trend favored the high pressure group.

Therefore, MAP may be an important intraoperative therapeutic hemodynamic target to reduce the incidence of complications in patients undergoing CPB.

Undersøgelsestype

Interventionel

Fase

  • Ikke anvendelig

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiesteder

  • Den Russiske Føderation
      • Novosibirsk, Den Russiske Føderation, 630055
        • Meshalkin Research Institute of Pathology of Circulation

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

18 år og ældre (Voksen, Ældre voksen)

Tager imod sunde frivillige

Ingen

Køn, der er berettiget til at studere

Alle

Beskrivelse

Inclusion Criteria:

  • ≥18 years old
  • Signed informed consent
  • Elective cardiac surgery under CPB (CABG or valve surgery)

Exclusion Criteria:

  • Unstable Coronary Artery Disease: Recent (< 6 weeks) myocardial infarction, unstable angina, severe (> 70%) left main coronary artery stenosis
  • Uncontrolled hypertension preoperatively (SBP > 160 mm Hg)
  • Critical preoperative state (ventricular tachycardia or ventricular fibrillation or aborted sudden death, preoperative cardiac massage, preoperative ventilation before anesthetic room, hemodynamic instability, preoperative inotropes or intraaortic balloon pumping, preoperative severe acute renal failure (anuria or oliguria <10ml/hr)
  • Planned surgery on aorta
  • Emergency surgery
  • Pregnancy
  • Current enrollment into another randomized controlled trial (in the last 30 days)
  • Previous enrollment and randomization into current study
  • Glomerular filtration rate ≤59 ml/min/1.73m2 (Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI) equation)

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Forebyggelse
  • Tildeling: Randomiseret
  • Interventionel model: Parallel tildeling
  • Maskning: Dobbelt

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Eksperimentel: Individualized BP group
Individualized intraoperative BP management
Andet: Individualized intraoperative BP management

In the treatment group, the nurse will measure resting blood pressure three times in the ward one day before surgery (after a 5-min rest while lying supine). Average measurement will be used to calculate mean arterial pressure (MAP).

Before and after CPB patients will receive continuous infusion of norepinephrine to maintain MAP within ± 10% of patients resting MAP. If targeted MAP during CPB could not be achieved after increasing pump-flow (not more than 130%), infusion of norepinephrine will used. After CPB, the choice of vasopressors/inotropes to maintain predefined MAP will be left on attending anesthesiologists based on patient status.
Placebo komparator: Standard treatment group
Standard intraoperative BP management
Andet: Standard intraoperative BP management
Standard treatment strategy will be used aiming to maintain pre-bypass and post-bypass MAP at 65-75 mm Hg. MAP during CPB will be maintained at 50-60 mm Hg. If MAP of 50-60 mm Hg during CPB could not be achieved after increasing pump-flow (not more than 130%), infusion of norepinephrine will be started. No vasodilators will be used if MAP will exceed predefined range.

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Compliance with the protocol
Tidsramme: Operative day 1
Successful compliance with protocol is defined as ≥ 90% of prescribed intervention being administered across all patients.
Operative day 1
Successful recruitment rate
Tidsramme: 12 month
Successful recruitment rate will be defined as recruitment of 2 patients per week.
12 month

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Postoperative creatinine concentration
Tidsramme: 3 days after surgery
Plasma creatinine level will be measured daily during 3 postoperative days.
3 days after surgery
Postoperative cardiac troponin I level
Tidsramme: 12 hours after surgery
Cardiac troponin I level wil be measured in the time frame from 6 to 12 hours postoperatively.
12 hours after surgery
Intraoperative blood pressure
Tidsramme: Operative day 1
Intraoperative blood pressure (mean, systolic and diastolic) will be registered every 5 minutes intraoperatively using invasive blood pressure monitoring system.
Operative day 1
Rate of postoperative complications
Tidsramme: 30 days after surgery
Postoperative complications (myocardial infarction, atrial fibrillation, stroke, delirium, need for renal replacement therapy, infection, reexploration for bleeding) will be defined according to standard European Society of Anaesthesiology/European Society of Intensive Care Medicine definitions where possible.
30 days after surgery
Postoperative blood loss
Tidsramme: Postoperative day 1
Drainage volume (ml/kg) will be measured in the next morning after surgery.
Postoperative day 1
Daily Sequential Organ Failure Assessment (SOFA) score
Tidsramme: 30 days after surgery
Organ failure will be assessed by using Sequential Organ Failure Assessment (SOFA) score which will be recorded daily until patient discharge from the ICU. The score is based on six different scores, one each for the respiratory, cardiovascular, hepatic, coagulation, renal and neurological systems. Each organ system is assigned a point value from 0 (normal) to 4 (high degree of dysfunction/failure). The score ranges from 0 to 24 points (the higher the score, the higher the mortality).
30 days after surgery
Peak concentration of lactate during CPB and up to 24 hours after surgery
Tidsramme: Postoperative day 1
Lactate values (mmol/l) will be measured every 6 hours during the first 24 postoperative hours.
Postoperative day 1
Oxygen delivery during CPB
Tidsramme: Operative day 1
Oxygen delivery during CPB will be calculated according to the standard formula (pump flow x O2 arterial content).
Operative day 1
Cerebral oxygenation (near infrared spectroscopy)
Tidsramme: Operative day1
Number of cerebral desaturations will be recorded intraoperatively.
Operative day1
Ventilation > 24 hours
Tidsramme: 30 days after surgery
Number of patients with duration of ventilation more than 24 h.
30 days after surgery
Duration of ICU stay and hospitalization
Tidsramme: 30 days after surgery
Number of postoperative days spent in the ICU and in the hospital will be counted.
30 days after surgery
30-day all-cause mortality
Tidsramme: 30 days after surgery
Number of patients who will die within 30-day after surgery from any cause
30 days after surgery
Need for blood transfusions
Tidsramme: 30 days after surgery
Number of patients who will need transfusions of any blood products (RBC, fresh frozen plasma, platelets, cryoprecipitate).
30 days after surgery

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Sponsor

Meshalkin Research Institute of Pathology of Circulation

Efterforskere

  • Ledende efterforsker: Vladimir Lomivorotov, MD, PhD, Meshalkin Research Institute of Pathology of Circulation

Publikationer og nyttige links

Den person, der er ansvarlig for at indtaste oplysninger om undersøgelsen, leverer frivilligt disse publikationer. Disse kan handle om alt relateret til undersøgelsen.

Generelle publikationer

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart (Faktiske)

21. januar 2019

Primær færdiggørelse (Forventet)

10. marts 2020

Studieafslutning (Forventet)

10. april 2020

Datoer for studieregistrering

Først indsendt

3. oktober 2018

Først indsendt, der opfyldte QC-kriterier

21. december 2018

Først opslået (Faktiske)

24. december 2018

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

22. november 2019

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

20. november 2019

Sidst verificeret

1. november 2019

Mere information

Begreber relateret til denne undersøgelse

Nøgleord

Andre undersøgelses-id-numre

  • 19

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