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Study on the Effects and Mechanisms of Inhaling Cool Oxygen on Gut Microbiota and Prognosis in Myocardial Infarction Patients

Study on the Effects and Mechanisms of Inhaling Cool Oxygen on Gut Microbiota and Prognosis in Myocardial Infarction Patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600118447
Enrollment
Unknown
Registered
2026-02-05
Start date
2026-02-10
Completion date
Unknown
Last updated
2026-02-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute ST-elevation myocardial infarction

Interventions

Cool Oxygen inhalation group:Wear an oxygen mask daily to inhale cool (16°C) oxygen for 8 hours, continuing for one week.
Room-temperature oxygen inhalation group:Wear an oxygen mask daily to inhale room-temperature oxygen for 8 hours, continuing for one week.

Sponsors

The First Affiliated Hospital of Harbin Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: (1) >=18 years of age; (2) Onset of symptoms (initial chest pain or tightness) =2 leads (>=0.1 mV in limb leads, >=0.2 mV in precordial leads V1-V3); (4) Pre-PCI TIMI flow grade =2 in the culprit vessel demonstrated by immediate post-PCI coronary angiography).

Exclusion criteria

Exclusion criteria: (1) Cardiac arrest or ventricular fibrillation before or after admission; (2) Uncontrolled acute left ventricular failure or pulmonary oedema; (3) Severe cardiogenic shock unresponsive to vasopressors; (4) Left main coronary artery disease or multivessel coronary artery disease (>=70% stenosis in at least two coronary arteries with diameter >=2.5mm); (5) History of myocardial infarction or coronary artery bypass grafting (CABG); (6) Severe valvular disease requiring surgical intervention; (7) Hypertrophic/restrictive cardiomyopathy; (8) Renal failure (eGFR <30 mL/min or requiring dialysis); (9) Hepatic failure (Child-Pugh Class C) or active hepatitis; (10) Severe respiratory disease (e.g., asthma, COPD, pulmonary embolism); (11) Malignant neoplasms or life expectancy <1 year; (12) Pregnant or lactating women; (13) Inability to participate in the study: dementia, psychiatric disorders, or inability to sign informed consent; (14) Concurrent participation in other interventional clinical trials.

Design outcomes

Primary

MeasureTime frame
Incidence of major adverse cardiovascular and cerebrovascular events;Severe complications of ST-segment elevation myocardial infarction;cardiac function;Infarct area;NT-proBNP;hs-cTnI;CK-MB;hs-CRP;Indicators of ventricular systolic and diastolic function;Wall Motion Score Index;Arrhythmia events;Heart rate variability;Fecal metagenomic testing;

Secondary

MeasureTime frame
Whole-blood single-cell sequencing;Plasma metabolomics testing;Oral metagenomic testing;

Countries

China

Contacts

Public ContactYue Li

The First Affiliated Hospital of Harbin Medical University

ly99ly@vip.163.com+86 131 0173 7579

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 15, 2026