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The protective effect of administration of sevoflurane during the entire procedure and pulmonary static inflation with hypothermia gas during cardiopulmonay bypass on lung function in patients undergo

The protective effect of administration of sevoflurane during the entire procedure and pulmonary static inflation with hypothermia gas during cardiopulmonay bypass on lung function in patients undergo

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-11001373
Enrollment
Unknown
Registered
2011-05-29
Start date
2011-03-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

mitral valve disease and aortic valve disease

Interventions

Group A:receiving sevoflurane (1 minimal alveolar concentration MAC) during the entire procedure and pulmonary static inflation with hypothermia gas(10 degree C).
Group B:receiving sevoflurane (1 MAC) during entire procedure and pulmonary static inflation with room temperature gas(24 degree C)
Group C:receiving propofol (4-6mg/kg?h) during the entire procedure and pulmonary static inflation with hypothermia gas(10 degree C).
Group D:receiving propofol (4-6mg/kg?h) during entire procedure and pulmonary static inflation with room temperature gas(24 degree C).

Sponsors

The 2nd affliated hospital of Harbin Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Male and female aged 40 to 70 years old; 2. ASA grade stage 3 to 4; 3. Able and willing to provide signed signed informed consent; 4. Have elective cardiac valve replacement.

Exclusion criteria

Exclusion criteria: 1. Left ventricular ejection fraction (EF) <40% in preoperative period; 2. With hypotension that needs inotropic drugs or mechine to sustain normal level in preoperative period; 3. With coronary heart disease, congestive heart failure, stage 3 to 4 of liver and kidney dysfunction, chronic obstructive pulmonary disease or other respiratory dysfunction, disease of central nerves system, abnormality of haemostasis; 5. Severe pulmonary hypertension, left-to-right shunts heart diseases; 6. Had been treated with percutaneous balloon, mitral valvotomy or other cardiovascular surgeries; 7. Treated with hypoglycemic agents, theophylline agents, immune potentiator or suppressive agents and non-steroidal anti-inflammatory drugs (NSAIDs) before surgery.

Design outcomes

Primary

MeasureTime frame
oxygenation index;Extravascular Lung Water Index;Respiratoryindex;proinflammatory factors;Pulmonary Vascular Permeability Index;lung compliance;

Secondary

MeasureTime frame
neutrophile cell count;socre of chest X-ray;Cardiac output index;

Countries

China

Contacts

Public ContactWenzhi LI
wenzhili9@126.com+86 451 86605028

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026