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โ† Trials
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Inhaled Nitric Oxide for High Amplitude Pulmonary Edema (HAPE)

RecruitingNAAges 18 Years - 65 YearsAllNovlead Inc.
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In plain words

What the trial is, and whether it could suit you

High Altitude Pulmonary Edema (HAPE) is a critical, non-cardiogenic pulmonary edema that manifests in high-altitude conditions, marked by the rapid onset of symptoms such as dyspnea, cough, frothy sputum, and cyanosis. It represents a significant cause of mortality among high-altitude illnesses due to its swift progression and elevated fatality rates if not addressed promptly. The pathophysiological mechanisms underlying HAPE include excessive hypoxic pulmonary vasoconstriction, increased permeability of the pulmonary vasculature, impaired clearance of fluid from the lungs, and systemic fluid retention. A pivotal factor in HAPE is pulmonary arterial hypertension (PAH), characterized by a progressive rise in pulmonary arterial pressure and resistance, which can ultimately lead to right heart failure. Recent developments in the management of HAPE have introduced inhaled nitric oxide (iNO)

Sign in to get the eligibility rules as simple questions to take to your doctor.

๐Ÿ“‹ Eligibility rules (as published)
Inclusion Criteria: 1. Individuals aged between 18 and 65 years. 2. A score on the Lake Louise Acute Mountain Sickness Scale ranging from 3 to 9 points, as outlined in Annex 2, recorded in 2018. 3. Chest X-ray findings that demonstrate either thickening of the lung texture bilaterally or the presence of nodular opacities in the lower regions of both lungs. 4. Capacity to provide informed consent in accordance with local regulatory requirements. Exclusion Criteria: 1. Confirmed contraindications for the use of nitric oxide include the following (refer to "5.3.4 NO Contraindications"): * Severe hypoplasia of the left heart or duct-dependent congenital heart disease; * Life-threatening congenital anomalies and congestive heart failure; * Congenital methemoglobinemia; * Severe hemorrhagic conditions, including intracranial hemorrhage, intraventricular hemorrhage, and pulmonary hemorrhage. 2. Severe left ventricular dysfunction, characterized by a left ventricular ejection fraction (LVEF) of less than 40%. 3. Pulmonary edema resulting from other cardiac, pulmonary, thoracic, or systemic disorders. 4. Coexistence with high altitude cerebral edema. 5. A history of lung malignancy, lung resection, or lung transplantation. 6. Barotrauma, which may include pneumothorax, subcutaneous and mediastinal emphysema, or the presence of a closed drainage tube in the thoracic cavity. 7. Clinically significant or persistent thrombocytopenia, defined as a platelet count of less than 50ร—10\^9/L. 8. Administration of pulmonary hypertension medications, such as sildenafil, bosentan, or prostacyclins, within the preceding 30 days. 9. Noncompliance with study protocols and unwillingness to provide informed consent. 10. Any other conditions that the clinician deems render the subject unsuitable for participation in the study.
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What it tests

  • Nitric Oxide Generation and Delivery System
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Where

1 site
Tibet Fokang Hospital
Lhasa, China
๐Ÿค Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible โ€” always decide together with your own doctor.
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