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NCT Number: NCT06950294

iNO300 Therapy in Critically Ill Patients With Pneumonia

The goal of this clinical trial is to learn the formation and recovery rate of methemoglobin (MetHb) in severely sick patients with pneumonia who receive high doses of inhaled nitric oxide (iNO) therapy at 250 parts per million (ppm), not exceeding 300 ppm. Meanwhile, the benefits of the therapy to treat severely sick patients with pneumonia will be explored. Patients who are 18 years or older, newly diagnosed with pneumonia, and severely sick with requirement of a breathing machine could be included. The main questions it aims to answer are:

How does methemoglobin change through the iNO treatment? Does iNO therapy increase the number of patients recovering from pneumonia? Researchers will compare iNO treatment to placebo, which means using the same device as the treatment group without delivering the study drug.

Participants will:

* Receive iNO treatment starting at 250 ppm, not exceeding 300 ppm, 40 min, every 6 hours, from day 1 to day 5 * Be followed up for 60 days

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Early Phase 1

Primary location

Massachusetts General Hospital

Boston, Massachusetts, 02114, United States

Location status: Recruiting

Location contact

Run Dong

CONTACT

[email protected]

6172563916

About this study

This study is designed as a pilot, double-blinded, randomized controlled trial to investigate levels of methemoglobin in the treatment group versus the control group and efficacy of high dose inhaled NO among critically ill patients with pneumonia. We will enroll 34 adult patients with newly diagnosed pneumonia and invasive mechanical ventilation who are admitted to the ICUs at Massachusetts General Hospital.

After enrollment, participants will be randomized in 1:1 ratio to intervention group or control group. Baseline characteristics will be collected.

During treatment period, patients allocated to the intervention group will receive high dose inhaled NO starting at 250 ppm (not exceeding 300 ppm), 40min, 4 times daily, for 5 days. The control group will receive sham intervention. Both groups will receive standard therapy.

During follow-up period, we will follow participants for a total duration of 60 days. Methemoglobin kinetic levels and efficacy outcomes will be collected.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 18 years or older
  • Intubated and mechanically ventilated
  • Within 72h of diagnosis of community- or hospital-acquired pneumonia
  • Written informed consent obtained from patients or legally authorized representatives

Exclusion criteria

  • Baseline methemoglobin 3% or higher
  • Genetic diseases including glucose-6-phosphate dehydrogenase deficiency, cytochrome b5 reductase deficiency, sickle cell disease
  • Oxygen saturation < 88% on 100% inspired fraction of oxygen
  • Anemia with hemoglobin < 7.0 g/dl
  • Acute cardiogenic shock requiring inotropic or mechanical support with an ejection fraction less than 20%
  • Receiving inhaled NO therapy or decision to initiate inhaled NO therapy within 24 hours post randomization
  • A decision to do-not-resuscitate (DNR)
  • Enrollment in another experimental antimicrobial treatment protocol
  • Patients for whom follow-up is expected to be impossible

Treatment and study plan

High dose inhaled nitric oxide

Drug

Inhaled nitric oxide starting at 250-300 ppm, 40min, every 6 hours, from day 1 to day 5. Nitric oxide is delivered using a gas cylinder containing nitric oxide and nitrogen.

Sham Treatment

Other

Sham intervention with the nitric oxide gas cylinder replaced by that containing only nitrogen and all other delivery procedures identical to the intervention group

Standard therapy

Other

Standard therapy pneumonia and critical illness

Primary outcomes

  1. Peaks of methomoglobin

    Time frame: From Day 1 to Day 5

    Continuous recording of MetHb and peaks of MetHb will be determined.

Secondary outcomes

  1. Nitrogen dioxide level

    Time frame: From Day 1 to Day 5

    Continuous measurement of nitrogen dioxide concentration in the inspiratory limb of breathing circuit

  2. Feasibility

    Time frame: From enrollment to Day 60

    Referral, recruitment, retention, compliance and follow-up completion rates of the study

  3. Clinical cure rate of pneumonia

    Time frame: From enrollment to test of cure day (4 -11 days post end of treatment)

    Clinical cure is assessed at test of cure (4 -11 days post end of treatment) and defined as resolution of clinical signs and symptoms of pneumonia compared with baseline, including a reduction in SOFA and CPIS scores, improvement or lack of progression in chest imaging, and no requirement for additional antibacterial treatment.

  4. Clinical improvement rate of pneumonia

    Time frame: Day 5

    Clinical improvement is assessed at end of treatment and defined as improvement in 2 or more clinical signs and symptoms of pneumonia compared with baseline, improvement or lack of progression of chest x-ray abnormalities, and no requirement for additional antibacterial treatment. Clinical signs and symptoms of pneumonia include new onset or worsening cough, purulent sputum or increased suction requirements, auscultation findings of pneumonia, dyspnea, tachypnea, or respiratory rate ≥ 30/min, hypoxemia, worsening gas exchange.

  5. Microbiologic eradication rate

    Time frame: From enrollment to test of cure day (4 -11 days post end of treatment)

    Absence of the baseline pathogen from tracheal aspiration or bronchoalveolar lavage fluid will be confirmed. If it is not possible to obtain an appropriate clinical specimen for culture and the patient has a successful clinical outcome, the response was presumed to be eradication.

  6. 28-day all cause mortality

    Time frame: From enrollment to Day 28

    All cause mortality from enrollment to Day 28

  7. 60-day all cause mortality

    Time frame: From enrollment to Day 60

    All cause mortality from enrollment to Day 60

  8. 28-day ventilator free days

    Time frame: From enrollment to Day 28

    Successful liberation from mechanical ventilation should last more than 48 h without re-intubation in patients who have survived 28 days after randomization (extubation was counted from the last successful attempt in patients who have survived 28 days since randomization) and for patients ventilated for 28 days or more or who died before 28 days (irrespective of intubation status), the number of ventilator-free days was recorded at zero.

  9. Days free from organ support in 28 days

    Time frame: From enrollment to Day 28

    Organ support includes mechanical ventilation, vasopressors and renal replacement therapy.

  10. Blood stream infection

    Time frame: From enrollment to Day 28

    Positive blood culture with a pathogenic bacterium

  11. Days free from antibiotics during hospitalization

    Time frame: From enrollment to the day of hospital discharge or death, whichever comes earlier, assessed up to 60 days

    Days free from antibiotics during hospitalization

  12. Acquisition of multidrug-resistant (MDR) infection or colonization

    Time frame: From enrollment to Day 28

    Multidrug-resistant infection is defined as pathogen acquiring non-susceptibility to at least one agent in three or more antibiotic categories

  13. Hospital stay

    Time frame: From enrollment to the day of hospital discharge or death, whichever comes earlier, assessed up to 60 days

    Days from enrollment to the end of hospitalization

  14. ICU length of stay

    Time frame: From enrollment to the day of ICU discharge or death, whichever comes earlier, assessed up to 60 days

    ICU length of stay

  15. Inflammatory markers

    Time frame: From enrollment to test of cure (4-11 days post end of treatment)

    The test includes C reactive protein (CRP), procalcitonin (PCT), monocyte chemoattractant protein-1 (MCP-1), tumor necrosis factor α (TNF α), interleukin 6 (IL-6), interleukin 8 (IL-8), interleukin 10 (IL-10).

  16. Relapse rate

    Time frame: From enrollment to Day 28

    Relapse is assessed for patients with hospital-acquired pneumonia at 28-day follow-up after test of cure and defined as recurrence or new appearance of at least two of the three symptoms and signs (fever greater than 38 °C, leukocytosis or leukopenia, and purulent tracheobronchial secretions), along with a new or persistent infiltrate on chest radiography in a patient assessed as clinical cure at TOC.

Study contacts

Contact information is provided by the study sponsor or research team.

Lorenzo Berra, MD

CONTACT

[email protected]

617-726-3030

Run Dong, MD

CONTACT

[email protected]

617-726-3030

Sponsors and collaborators

Lead sponsor

Massachusetts General Hospital

Other

Registry information

Official study title

High Dose Inhaled Nitric Oxide Therapy in Critically Ill Patients With Pneumonia: a Pilot, Double-blinded, Randomized, Controlled Trial

Acronym: iNO300

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Apr 30, 2025
Registry last updated
May 22, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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