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The effects of different ventilation modes on patients with coronary heart disease during one-lung ventilation pneumonectomy

The effects of different ventilation modes on patients with coronary heart disease during one-lung ventilation pneumonectomy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-OOC-16009112
Enrollment
Unknown
Registered
2016-08-29
Start date
2016-10-07
Completion date
Unknown
Last updated
2018-03-12

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

Conditions

The use of ventilation modes

Interventions

VCV:Volume control ventilation
lung protective ventilation group:lung protective ventilation

Sponsors

Beijing Anzhen Hospital Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
25 Years to 70 Years

Inclusion criteria

Inclusion criteria: Patients scheduled for surgery under general anesthesia were eligible if they either (1) had proven CAD and were scheduled for pneumonectomy or (2) had =2 risk factors for CAD and were scheduled for pneumonectomy Proof of CAD was predefined as a history of myocardial infarctionor coronary revascularization, or a >50% stenosis on coronary angiography, or myocardial ischemia induced by radionuclide or echocardiographic stress testing. The predefined risk factors for CAD were age =70 years, diabetes mellitus requiring treatment (oral antidiabetic medications or insulin), arterial hypertension, history of stroke, functional capacity<4metabolic equivalent task, absence of sinus rhythm, and abnormal ECG (signs of left ventricular hypertrophy, left bundle branch block,or abnormalities of the ST-segment or T-wave).

Exclusion criteria

Exclusion criteria: We excluded patients in case of the following: (1) current medication with sulfonylurea derivatives or theophylline unless stopped =2 days before surgery because these drugs reportedly inhibit anesthetic preconditioning; (2) current congestive heart failure; (3) current unstable angina pectoris; (4) preoperative hemodynamic instability, defined as the use of vasopressors; (5) hepatic disease, defined as alanine aminotransferase and/or aspartate aminotransferase values >100 U/L; (6) renal insufficiency, defined as creatinine clearance >30 mL/min; (7) emergent surgery; (8) severe chronic obstructive pulmonary disease, defined as forced expiratory volume in the first second of expiration<1 L; (9) prior enrollment in the study; (10) concurrent enrollment in another RCT; (11) pregnancy; or (12) absence of written informed consent.

Design outcomes

Primary

MeasureTime frame
pH;PO2;PCO2;VT;Ppeak;Pplat;Pmean;Cdyn;Raw;

Secondary

MeasureTime frame
HR;CVP;MAP;PV;MACC;CO;SV;FLTc;FLT;CI;TSVR;interleukin(IL)-6;tumor necrosis factor-a;COR;Blood sugar;Lactic acid;MPO;MDA;C-reactive protein;Troponin T;CK-MB;NT-proBNP;miRNAs;ECG;

Countries

China

Contacts

Public ContactJun Ma

Beijing Anzhen Hospital Capital Medical University

majun7689@163.com+86 010-64456779

Outcome results

None listed

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