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Inhaled NO in Surgical Patients With Recent COVID-19 Infection (INORDINATE)

Primary Purpose

Nitric Oxide, COVID-19, Surgery

Status
Recruiting
Phase
Phase 2
Locations
China
Study Type
Interventional
Intervention
Nitric Oxide Gas
Sponsored by
Xijing Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Nitric Oxide focused on measuring Nitric Oxide Inhalation, Postoperative Pulmonary Complications, Surgery, COVID-19

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: ≥ 18 years old Planned for surgery under general anesthesia With a history of COVID-19 infection within 7 weeks prior to surgery. Exclusion Criteria: Physician makes a decision that trial involvement is not in the patient's best interest or any condition that does not allow the protocol to be followed safely ASA ≥ IV, life expectancy< 24 h. Pregnant or lactating women. Severe liver disease (Child-Pugh score ≥ 12). Patients with severe respiratory failure need mechanical ventilation support or ECMO life support before the operation. Severe renal dysfunction (eGFRC≤30 ml/min/1.73m2) or receiving continuous renal replacement therapy, hemodialysis, and peritoneal dialysis. Having received or participated in other clinical trials within the previous month.

Sites / Locations

  • Xijing HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Experimental: Treatment Group

Sham Comparator: Control Group

Arm Description

Inspired NO/N2 will be delivered at 80 parts per million (ppm) after anesthesia induction and intubation and lasted until the end of surgery and leave the operating room. The physician will follow their own institutional weaning protocols.

The delivery system will be set up anyway without studying gas administration

Outcomes

Primary Outcome Measures

postoperative pulmonary complications
It is composite outcome including respiratory infection, respiratory failure, pleural effusion, atelectasis, pneumothorax, bronchospasm, and aspiration pneumonitis

Secondary Outcome Measures

mortality within 30 days postoperatively
All-cause mortality
Classification of pulmonary complications (Clavien-Dindo)
Evaluation of the severity of pulmonary complications according to Clavien-Dindo classification. It consists of 7 grades (I, II, IIIa, IIIb, IVa, IVb and V).
the rate of unplanned ICU admission
Percentage of patients admitted into ICU after surgery, which is not expected before surgery
postoperative length of hospital stay
duration between end of surgery and discharge from hospital
Incidence of thrombotic events
including DVT and pulmonary embolism
incidence of nonpulmonary complications
including acute kidney injury, Stroke and myocardial infarction
postoperative comprehensive complication index (CCI)
Ranging from 0 (no complication) to 100 (death) was computed based on the Clavien-Dindo classification

Full Information

First Posted
February 7, 2023
Last Updated
February 17, 2023
Sponsor
Xijing Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT05721144
Brief Title
Inhaled NO in Surgical Patients With Recent COVID-19 Infection
Acronym
INORDINATE
Official Title
Inhaled NO ReDuce postoperatIve pulmoNAry complicATions in patiEnts With Recent COVID-19 Infection
Study Type
Interventional

2. Study Status

Record Verification Date
February 2023
Overall Recruitment Status
Recruiting
Study Start Date
February 17, 2023 (Actual)
Primary Completion Date
December 31, 2023 (Anticipated)
Study Completion Date
January 31, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Xijing Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The aim of this study is to evaluate the effect of perioperative inhalation of NO on reducing the incidence of postoperative pulmonary complications in patients with recent COVID-19 infection, and to evaluate whether inhaled NO can improve the prognosis of patients. The investigators will enroll 660 surgical patients who was infected with SARS-CoV-2 within 42days (7 weeks ) prior to planed surgery under general anesthesia. Patients will be randomized to receive either inhaled nitric oxide (per protocol) or a placebo. Perioperative standards of care will be the institution's own protocols (such as ventilation strategies and use and dose of anesthetics, analgesia and fluid management, etc).
Detailed Description
The outbreak of COVID-19 and its global pandemic has posed a threat to public health. On December 7, 2022, the National Health Commission (NHC) of China issued an announcement on further optimization of public health control measures. Since then, the rapid spread and breakthrough of SARS-CoV-2 infections have been observed in the majority of China, caused by the more infectious and less virulent Omicron variant of SARS-Cov-2. Consequently, the proportion of surgical patients with current or previous SARS-CoV-2 infections will inevitably increase within a relatively narrow time window. It has been reported that a history of SARS-CoV-2 infection is associated with a transiently elevated risk of postoperative complications. The longer the time interval between infection and surgery, the lower the risk of postoperative complications. An updated recommendation suggested postponing surgery for at least seven weeks following SARS-CoV-2 infection, thereby reducing the risk of postoperative complications and 30-day mortality to baseline levels (similar to those without a history of SARS-CoV-2 infection). COVID-19 infection significantly affects respiratory functions by massively disrupting pulmonary oxygenation and activating the synthesis of proinflammatory cytokines, inducing severe oxidative stress, enhanced vascular permeability, and endothelial dysfunction which has rendered researchers and clinicians to depend on prophylactic treatment due to the unavailability of proper disease management approaches. Inhaled nitric oxide gas (NO) has shown antiviral activity against Coronavirus during the 2003 SARS outbreak. Previous studies have indicated that nitric oxide (NO) application appears to be significant concerning the antiviral activities, antioxidant, and anti-inflammatory properties in relieving disease-related symptoms. Inhaled nitric oxide had been widely used during the Covid-19 pandemic. In the scoping and systemic reviews, it was demonstrated that nitric oxide inhalation was effective in improving oxygenation, cardiopulmonary function, and fastening virus clearance. The investigators designed this study to assess whether inhaled NO reduces postoperative pulmonary complications in patients with a COVID-19 infection history 7 weeks prior to surgery. Here, the investigators propose a randomized clinical trial aimed to improve postoperative outcomes in patients with an increased risk of postoperative pulmonary complications after COVID-19 infection. Control group: the institutional standard of care will be delivered. Treatment group: In addition to standard therapy, the subjects will receive inhalation of NO. Inspired NO/N2 will be delivered at 80 parts per million (ppm) after anesthesia induction and intubation and last until the end of surgery and leave the operating room. The physician will follow their own institutional weaning protocols. In the absence of institutional protocols, NO will be reduced in a step-wise fashion starting from 40 ppm to 20, 10, 5, 3, 2, and 1 ppm. If hypoxemia (SpO2 < 93%) or acute hypotension (systolic blood pressure < 90 mmHg) occurs during weaning, NO should be increased to a prior higher concentration. Safety: prolonged treatment with inhaled NO can lead to increased methemoglobin levels. Blood levels of methemoglobin will be monitored via a non-invasive CO-oximeter or MetHb levels in the blood. If methemoglobin levels rise above 5% at any point in the study, inhaled NO concentration will be halved.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Nitric Oxide, COVID-19, Surgery, Postoperative Complications
Keywords
Nitric Oxide Inhalation, Postoperative Pulmonary Complications, Surgery, COVID-19

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
660 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Experimental: Treatment Group
Arm Type
Experimental
Arm Description
Inspired NO/N2 will be delivered at 80 parts per million (ppm) after anesthesia induction and intubation and lasted until the end of surgery and leave the operating room. The physician will follow their own institutional weaning protocols.
Arm Title
Sham Comparator: Control Group
Arm Type
No Intervention
Arm Description
The delivery system will be set up anyway without studying gas administration
Intervention Type
Drug
Intervention Name(s)
Nitric Oxide Gas
Other Intervention Name(s)
Nitric Oxide inhalation
Intervention Description
Inspired NO/N2 will be delivered at 80 parts per million (ppm) after anesthesia induction and intubation and lasted until the end of surgery and leave the operating room.
Primary Outcome Measure Information:
Title
postoperative pulmonary complications
Description
It is composite outcome including respiratory infection, respiratory failure, pleural effusion, atelectasis, pneumothorax, bronchospasm, and aspiration pneumonitis
Time Frame
within 7 days after operation
Secondary Outcome Measure Information:
Title
mortality within 30 days postoperatively
Description
All-cause mortality
Time Frame
within 30 days after operation
Title
Classification of pulmonary complications (Clavien-Dindo)
Description
Evaluation of the severity of pulmonary complications according to Clavien-Dindo classification. It consists of 7 grades (I, II, IIIa, IIIb, IVa, IVb and V).
Time Frame
within 7 days after operation
Title
the rate of unplanned ICU admission
Description
Percentage of patients admitted into ICU after surgery, which is not expected before surgery
Time Frame
within 7 days after operation
Title
postoperative length of hospital stay
Description
duration between end of surgery and discharge from hospital
Time Frame
From the date of surgery until the date patient discharge from hospital, assessed up to 30 days
Title
Incidence of thrombotic events
Description
including DVT and pulmonary embolism
Time Frame
From the date of surgery until the date patient discharge from hospital, assessed up to 30 days
Title
incidence of nonpulmonary complications
Description
including acute kidney injury, Stroke and myocardial infarction
Time Frame
From the date of surgery until the date patient discharge from hospital, assessed up to 30 days
Title
postoperative comprehensive complication index (CCI)
Description
Ranging from 0 (no complication) to 100 (death) was computed based on the Clavien-Dindo classification
Time Frame
within 7 days after operation
Other Pre-specified Outcome Measures:
Title
Incidence of hypotension
Description
It is diagnosed as SBP < 90mmHg or drop ≥ 30% of baseline lasted for 5 min
Time Frame
From anesthesia induction until leave operation room, assessed up to 12 hrs
Title
Incidence of hypertension
Description
It is diagnosed as SBP > 180 mmHg or rise ≥ 30% of baseline lasted for 5 min
Time Frame
During surgery, from anesthesia induction to end of anesthesia
Title
Occurrence of arrhythmia
Description
consisted of bradycardia (HR < 40bpm) or tachycardia (HR> 100 bpm) or new onset of arrhythmia that require Anti-arrhythmic drugs
Time Frame
From anesthesia induction until leave operation room, assessed up to 12 hrs
Title
Incidence of airway hyperresponsiveness
Description
airway peak pressure > 40 cm water
Time Frame
From anesthesia induction until leave operation room, assessed up to 12 hrs
Title
Number that the concentration of NO was adjusted
Description
For safety, if the N2O or metHb level exceed safety threshold, the NO concentration needs to be adjusted. The number of adjustment is recorded
Time Frame
During NO inhalation, from anesthesia induction until leave operation room, assessed up to 12 hrs
Title
massive bleeding
Description
bleeding exceed 1000 ml
Time Frame
From anesthesia induction until leave operation room, assessed up to 12 hrs

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: ≥ 18 years old Planned for surgery under general anesthesia With a history of COVID-19 infection within 7 weeks prior to surgery. Exclusion Criteria: Physician makes a decision that trial involvement is not in the patient's best interest or any condition that does not allow the protocol to be followed safely ASA ≥ IV, life expectancy< 24 h. Pregnant or lactating women. Severe liver disease (Child-Pugh score ≥ 12). Patients with severe respiratory failure need mechanical ventilation support or ECMO life support before the operation. Severe renal dysfunction (eGFRC≤30 ml/min/1.73m2) or receiving continuous renal replacement therapy, hemodialysis, and peritoneal dialysis. Having received or participated in other clinical trials within the previous month.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Chong Lei, MD, phd
Phone
86-18629011362
Email
crystalleichong@126.com
First Name & Middle Initial & Last Name or Official Title & Degree
Lini Wang, MD
Phone
86-15209234508
Email
wangln238@163.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Chong Lei, MD&phD
Organizational Affiliation
Xijing Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Xijing Hospital
City
Xi'an
State/Province
Shaanxi
ZIP/Postal Code
710032
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Chong Lei, MD & phD
Phone
86-18629011362
Email
crystalleichong@126.com
First Name & Middle Initial & Last Name & Degree
lini Wang, MD
Phone
86-15209234508
Email
wangln238@163.com

12. IPD Sharing Statement

Citations:
PubMed Identifier
32031570
Citation
Wang D, Hu B, Hu C, Zhu F, Liu X, Zhang J, Wang B, Xiang H, Cheng Z, Xiong Y, Zhao Y, Li Y, Wang X, Peng Z. Clinical Characteristics of 138 Hospitalized Patients With 2019 Novel Coronavirus-Infected Pneumonia in Wuhan, China. JAMA. 2020 Mar 17;323(11):1061-1069. doi: 10.1001/jama.2020.1585. Erratum In: JAMA. 2021 Mar 16;325(11):1113.
Results Reference
background
PubMed Identifier
31978945
Citation
Zhu N, Zhang D, Wang W, Li X, Yang B, Song J, Zhao X, Huang B, Shi W, Lu R, Niu P, Zhan F, Ma X, Wang D, Xu W, Wu G, Gao GF, Tan W; China Novel Coronavirus Investigating and Research Team. A Novel Coronavirus from Patients with Pneumonia in China, 2019. N Engl J Med. 2020 Feb 20;382(8):727-733. doi: 10.1056/NEJMoa2001017. Epub 2020 Jan 24.
Results Reference
background
PubMed Identifier
32085846
Citation
Xu Z, Shi L, Wang Y, Zhang J, Huang L, Zhang C, Liu S, Zhao P, Liu H, Zhu L, Tai Y, Bai C, Gao T, Song J, Xia P, Dong J, Zhao J, Wang FS. Pathological findings of COVID-19 associated with acute respiratory distress syndrome. Lancet Respir Med. 2020 Apr;8(4):420-422. doi: 10.1016/S2213-2600(20)30076-X. Epub 2020 Feb 18. No abstract available. Erratum In: Lancet Respir Med. 2020 Feb 25;:
Results Reference
background
PubMed Identifier
15546092
Citation
Chen L, Liu P, Gao H, Sun B, Chao D, Wang F, Zhu Y, Hedenstierna G, Wang CG. Inhalation of nitric oxide in the treatment of severe acute respiratory syndrome: a rescue trial in Beijing. Clin Infect Dis. 2004 Nov 15;39(10):1531-5. doi: 10.1086/425357. Epub 2004 Oct 22.
Results Reference
background
PubMed Identifier
15234326
Citation
Keyaerts E, Vijgen L, Chen L, Maes P, Hedenstierna G, Van Ranst M. Inhibition of SARS-coronavirus infection in vitro by S-nitroso-N-acetylpenicillamine, a nitric oxide donor compound. Int J Infect Dis. 2004 Jul;8(4):223-6. doi: 10.1016/j.ijid.2004.04.012.
Results Reference
background
PubMed Identifier
35852269
Citation
Valsecchi C, Winterton D, Safaee Fakhr B, Collier AY, Nozari A, Ortoleva J, Mukerji S, Gibson LE, Carroll RW, Shaefi S, Pinciroli R, La Vita C, Ackman JB, Hohmann E, Arora P, Barth WH Jr, Kaimal A, Ichinose F, Berra L; DELiverly oF iNO (DELFiNO) Network Collaborators. High-Dose Inhaled Nitric Oxide for the Treatment of Spontaneously Breathing Pregnant Patients With Severe Coronavirus Disease 2019 (COVID-19) Pneumonia. Obstet Gynecol. 2022 Aug 1;140(2):195-203. doi: 10.1097/AOG.0000000000004847. Epub 2022 Jul 6.
Results Reference
background
PubMed Identifier
33347987
Citation
Fang W, Jiang J, Su L, Shu T, Liu H, Lai S, Ghiladi RA, Wang J. The role of NO in COVID-19 and potential therapeutic strategies. Free Radic Biol Med. 2021 Feb 1;163:153-162. doi: 10.1016/j.freeradbiomed.2020.12.008. Epub 2020 Dec 22.
Results Reference
background
PubMed Identifier
36192801
Citation
Al Sulaiman K, Korayem GB, Altebainawi AF, Al Harbi S, Alissa A, Alharthi A, Kensara R, Alfahed A, Vishwakarma R, Al Haji H, Almohaimid N, Al Zumai O, Alrubayan F, Asiri A, Alkahtani N, Alolayan A, Alsohimi S, Melibari N, Almagthali A, Aljahdali S, Alenazi AA, Alsaeedi AS, Al Ghamdi G, Al Faris O, Alqahtani J, Al Qahtani J, Alshammari KA, Alshammari KI, Aljuhani O. Evaluation of inhaled nitric oxide (iNO) treatment for moderate-to-severe ARDS in critically ill patients with COVID-19: a multicenter cohort study. Crit Care. 2022 Oct 3;26(1):304. doi: 10.1186/s13054-022-04158-y.
Results Reference
background
PubMed Identifier
33288208
Citation
Garfield B, McFadyen C, Briar C, Bleakley C, Vlachou A, Baldwin M, Lees N, Price S, Ledot S, McCabe C, Wort SJ, Patel BV, Price LC. Potential for personalised application of inhaled nitric oxide in COVID-19 pneumonia. Br J Anaesth. 2021 Feb;126(2):e72-e75. doi: 10.1016/j.bja.2020.11.006. Epub 2020 Nov 14. No abstract available.
Results Reference
background
PubMed Identifier
35530860
Citation
Ghosh A, Joseph B, Anil S. Nitric Oxide in the Management of Respiratory Consequences in COVID-19: A Scoping Review of a Different Treatment Approach. Cureus. 2022 Apr 5;14(4):e23852. doi: 10.7759/cureus.23852. eCollection 2022 Apr.
Results Reference
background
PubMed Identifier
35599794
Citation
Bunch CM, Moore EE, Moore HB, Neal MD, Thomas AV, Zackariya N, Zhao J, Zackariya S, Brenner TJ, Berquist M, Buckner H, Wiarda G, Fulkerson D, Huff W, Kwaan HC, Lankowicz G, Laubscher GJ, Lourens PJ, Pretorius E, Kotze MJ, Moolla MS, Sithole S, Maponga TG, Kell DB, Fox MD, Gillespie L, Khan RZ, Mamczak CN, March R, Macias R, Bull BS, Walsh MM. Immuno-Thrombotic Complications of COVID-19: Implications for Timing of Surgery and Anticoagulation. Front Surg. 2022 May 4;9:889999. doi: 10.3389/fsurg.2022.889999. eCollection 2022.
Results Reference
background
PubMed Identifier
34428858
Citation
COVIDSurg Collaborative; GlobalSurg Collaborative. SARS-CoV-2 infection and venous thromboembolism after surgery: an international prospective cohort study. Anaesthesia. 2022 Jan;77(1):28-39. doi: 10.1111/anae.15563. Epub 2021 Aug 24.
Results Reference
background
PubMed Identifier
34793350
Citation
COVIDSurg Collaborative. Outcomes and Their State-level Variation in Patients Undergoing Surgery With Perioperative SARS-CoV-2 Infection in the USA: A Prospective Multicenter Study. Ann Surg. 2022 Feb 1;275(2):247-251. doi: 10.1097/SLA.0000000000005310.
Results Reference
background
PubMed Identifier
34148733
Citation
Abbott TEF, Fowler AJ, Dobbs TD, Gibson J, Shahid T, Dias P, Akbari A, Whitaker IS, Pearse RM. Mortality after surgery with SARS-CoV-2 infection in England: a population-wide epidemiological study. Br J Anaesth. 2021 Aug;127(2):205-214. doi: 10.1016/j.bja.2021.05.018. Epub 2021 Jun 11.
Results Reference
background
PubMed Identifier
33690889
Citation
COVIDSurg Collaborative; GlobalSurg Collaborative. Timing of surgery following SARS-CoV-2 infection: an international prospective cohort study. Anaesthesia. 2021 Jun;76(6):748-758. doi: 10.1111/anae.15458. Epub 2021 Mar 9.
Results Reference
background
PubMed Identifier
35194788
Citation
El-Boghdadly K, Cook TM, Goodacre T, Kua J, Denmark S, McNally S, Mercer N, Moonesinghe SR, Summerton DJ. Timing of elective surgery and risk assessment after SARS-CoV-2 infection: an update: A multidisciplinary consensus statement on behalf of the Association of Anaesthetists, Centre for Perioperative Care, Federation of Surgical Specialty Associations, Royal College of Anaesthetists, Royal College of Surgeons of England. Anaesthesia. 2022 May;77(5):580-587. doi: 10.1111/anae.15699. Epub 2022 Feb 22.
Results Reference
background
PubMed Identifier
34689990
Citation
Mavrothalassitis O, Pirracchio R, Fong N, Lazzareschi D, Sharma A, Vaughn MT, Mathis M, Legrand M. Outcome of surgical patients during the first wave of the COVID-19 pandemic in US hospitals. Br J Anaesth. 2022 Jan;128(1):e35-e37. doi: 10.1016/j.bja.2021.09.023. Epub 2021 Oct 1. No abstract available.
Results Reference
background
PubMed Identifier
33864692
Citation
Wijeysundera DN, Khadaroo RG. Surgery after a previous SARS-CoV-2 infection: data, answers and questions. Anaesthesia. 2021 Jun;76(6):731-735. doi: 10.1111/anae.15490. Epub 2021 Apr 17. No abstract available.
Results Reference
background
PubMed Identifier
35277245
Citation
Lieberman N, Racine A, Nair S, Semczuk P, Azimaraghi O, Freda J, Eikermann M, Wongtangman K. Should asymptomatic patients testing positive for SARS-CoV-2 wait for elective surgical procedures? Br J Anaesth. 2022 May;128(5):e311-e314. doi: 10.1016/j.bja.2022.02.005. Epub 2022 Feb 16. No abstract available.
Results Reference
background
PubMed Identifier
34148732
Citation
Dobbs TD, Gibson JAG, Fowler AJ, Abbott TE, Shahid T, Torabi F, Griffiths R, Lyons RA, Pearse RM, Whitaker IS. Surgical activity in England and Wales during the COVID-19 pandemic: a nationwide observational cohort study. Br J Anaesth. 2021 Aug;127(2):196-204. doi: 10.1016/j.bja.2021.05.001. Epub 2021 Jun 18.
Results Reference
background

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Inhaled NO in Surgical Patients With Recent COVID-19 Infection

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