Nitric Oxide for Reduced Intensive Support in Cardiac Surgery With Cardiopulmonary Bypass

Trial statusRecruiting
Trial phasePhase 3
Trial typeInterventional
Biological sexAll
Age18+
SponsorXijing Hospital

About this trial

Cardiac surgery is a procedure that is commonly performed worldwide. Despite these technological advances, cardiac surgery remains a high-risk surgery. Among post-operative complications, acute kidney injury, respiratory failure, myocardial infarction, and stroke as well as cognitive dysfunction are significant causes of mortality in patients undergoing and following cardiac surgery. Inhaled nitric oxide (NO) therapy as a selective pulmonary vasodilator in cardiac surgery has been one of the most significant pharmacological advances in managing pulmonary hemodynamics and life threatening right ventricular dysfunction and failure. In addition, newer applications show greater promise of inhaled NO as a therapy in the area of cardiac surgery associated acute kidney injury and ischemia reperfusion. However, this remarkable expectation to inhaled NO has experienced a roller-coaster ride with high hopes and nearly universal demonstration of physiological benefits but disappointing translation of these benefits to harder clinical outcomes, like mortality. Most of our understanding on the iNO field in cardiac surgery stems from small observational or single center randomized trials, which failed to ascertain strong evidence base. As a consequence, there are only week clinical practice guidelines on the field and only European expert opinion for the use of iNO in routine and more specialized cardiac surgery. There is need for a large multicenter randomized controlled study to confirm the administration of iNO as an effective weapon for the battle against life threatening complication in high risk cardiac surgical patients.

In a previous meta analysis with 27 studies included, we demonstrated that inhaled nitric oxide (NO) could reduce the duration of mechanical ventilation and reducing biomarkers of organ injury and clinical signs of organ dysfunction in cardiac surgery under cardiopulmonary bypass (CPB) , but had no significance in the ICU stay, hospital stay, and mortality. This may be attributed to the small sample size of the most included studies (of the 27 studies included, 20 studies with sample size less than 100) and heterogeneity in timing, dosage and duration of iNO administration. Well-designed, large-scale, multicenter clinical trials are needed to further explore the effect of iNO in improving postoperative prognosis in cardiovascular surgical patients.

We are planning a large multicenter controlled randomized trial to demonstrate that inhaled nitric oxide can reduce composite outcome of death and Major Adverse Events (MAEs), including need for intensive supports due to heart failure, low cardiac output sydrome, or renal failure, respiratory failure, etc., and myocardial infarction, stroke, and sepsis at 30 days after surgery from 20% to 16% in patient undergoing cardiac surgery with cardiopulmonary bypass.

If the hypothesis had been proved and validated, the results of this study can provide strong evidence for guidelines to facilitate the routine use of iNO in all cardiopulmonary bypass assisted cardiac procedures with 31,800 postoperative outcomes improved per year in US and in China.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age ≥18 years.

Elective cardiac or aortic surgery requiring CPB

Without history of previous open heart surgery.

Disqualifiers

Immediate emergency cardiac surgery;

Cardiac surgery that requires deep hypothermic circulatory arrest;

Planned cardiac surgery for congenital heart disease repair;

Planned for heart transplatation

Trial design

Design model

Parallel

Treatments tested in this trial

  • Nitric Oxide Gas

    Drug

    Patients will receive 80 parts per million (ppm) NO during CPB through the oxygenator. After weaning of CPB, test gases will be delivered via inspiration limb of ventilator at a dose range of 40-80 ppm until 6 hours after ICU admission or until extubation after surgery, whichever comes first.

  • Standard Care Arm

    Drug

    Patients in this group will receive standard care and 80 ppm nitrogen (N2, control group) are added to the gas mixture as control. In the circumstances when the N2 is not applicable, such as when the plasma-chemical NO synthesis device is employed for NO generatiaon and delivery, the device will be connected to the CPB and ventilator circuits, but the synthesis will remain inactive in the control group. Consequently, the circuit will be supplied with air devoid of NO.

Treatment groups

3,650 Participants
are divided into 2 treatment groups
Group A: Intervention: iNO GroupExperimental treatment 1 intervention
Group B: Standard Care/Control GroupPlacebo comparator 1 intervention

Trial outcomes

Primary outcomes

1

Composite outcome of death and major adverse events requiring intensive life supports

It is composite outcome including: * all cause mortality; * ischemic events(myocardial infarction, ischemic stroke, and pulmonary embolism) , * Cardiac arrest that had been successfully resuscitated or new onset of acute cardiac failure (low output syndrome) requiring IABP, ECMO, left ventricular assist device, cardiac dysfunction need for large dose of inotrope support, ---Stage 3 AKI or Renal failure that required renal replacement therapy, * prolonged mechanical ventilation (\> 24h ), * re-sternotomy for any indication, * major arrhythmia ((Ventricular fibrilliation or ventricular tachycardia after weaning-off cardiopulmonary bypass, new onset atrial fibrillation requiring anticoagulant therapy or other intervention upon discharge from the hospital); * sepsis

Time frame
within 30 days after operation

Secondary outcomes

1

Total number of major adverse events (MAEs)

Total number of major adverse events( MAEs) listed as the components of the primary outcomes.

Time frame
within 30 days after operation
2

Incidence of the MAEs

Incidence of the MAEs listed as the components of the primary outcomes.

Time frame
within 30 days after operation
3

All AKI incidence

AKI incidence which will be diagnosed by KDIGO criteria

Time frame
within 7 days of surgery
4

Length of mechanical ventilation

Length of mechanical ventilation in hours

Time frame
within 30 days after operation

Other outcomes

1

Blood transfusion

Amount of each type of blood product transfused (red blood cells, fresh frozen plasma, platelets)

Time frame
during postoperative hospitalization, with an average of 10 days
2

Blood loss

Total amount of blood loss (chest tube drainage) in ml

Time frame
during the first 72 hours after surgery
3

Incidence of prolonged cardiovascular support

cardiovascular support by using inotropes for more than 48 hours

Time frame
during postoperative hospitalization, with an average of 10 days.
4

Maximum vasoactive-inotropic score (VIS)

The VIS will be calculated using the formula: Dopamine dose (mcg/Kg/min) + Dobutamine dose (mcg/Kg/min) + 100 x Epinephrine dose (mcg/Kg/min) + 100 x Norepinephrine dose (mcg/Kg/min) + 50 x Levosimendan dose (mcg/Kg/min) + Enoximone dose (mcg/Kg/min) + 10.000 x Vasopressin dose (UI/kg/min). The maximum VIS will be recorded each day.

Time frame
record the maximun of the day for the first 7 days after surgery

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Xijing Hospital

Lead sponsor

Nikolay O. Kamenshchikov., M.D., Tomsk National Research Medical Center of the Russian Academy of Sciences

Collaborator

Lorenzo Berra., M.D., Massachusetts General Hospital

Collaborator

Jiange Han, Tianjin Chest Hospital, Tianjin, China

Collaborator

Qingping Wu, Wuhan Union Hospital, Wuhan, China

Collaborator

Evgeniy Grigoriev, Research Institute for Complex Issues of Cardiovascular Diseases, Kemerovo, Russian Federation

Collaborator

Vladimir Boboshko, E. Meshalkin National Medical Research Center, Novosibirsk, Russian Federation

Collaborator

Andrei Bautin, The Almazov National Medical Research Centre, St. Petersburg, Russian Federation

Collaborator

Vladimir Pichugin, Specialized Cardiac Surgery Clinical Hospital named after Academician B.A. Korolev, Nizhny Novgorod, Russian Federation

Collaborator

Evgeniy Rosseykin, Federal Center of Cardiovascular Surgery, Khabarovsk, Russian Federation

Collaborator

Jing Shi, The Afffliated Hospital of Guizhou Medical University, Guiyang, China.

Collaborator

Grigoryev Evgeny, Scientific Research Insitute for Complex Issues of Cardiovascular Diseases, Kemerovo, Russia.

Collaborator

Mikhail Vasilev, Meshalkin National Medical Research Center, Мeshalkin of the ministry of health of the Russian Federation,Novosibirsk,Russia.

Collaborator

Jia Min, The First Affiliated Hospital of Nanchang University, Nanchang, China.

Collaborator

Jiawan Wang, Beijing Chao-Yang Hospital, Capital Medical University, Beijing, China

Collaborator

Zongbin Song, Xiangya Hospital, Central South University, Changsha, China.

Collaborator