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Protective effect of remote ischemic preconditioning combined with sevoflurane posttreatment on myocardial injury during laparoscopic radical resection of colorectal cancer

Protective effect of remote ischemic preconditioning combined with sevoflurane posttreatment on myocardial injury during laparoscopic radical resection of colorectal cancer

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100043313
Enrollment
Unknown
Registered
2021-02-10
Start date
2021-04-01
Completion date
Unknown
Last updated
2021-06-07

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

Conditions

Laparoscopic radical resection of colorectal cancer

Interventions

total intravenous anesthesia:Propofol anesthesia
Sevoflurane posttreatment:Sevoflurane anesthesia
Propofol combined with sevoflurane anesthesia:Propofol combined with sevoflurane anesthesia
RIPC and propofol anesthesia:Remote ischemic preconditioning and propofol anesthesia
RIPC and sevoflurane posttreatment:Remote ischemic preconditioning and sevoflurane anesthesia
RIPC and propofol combined with sevoflurane anesthesia:Remote ischemic preconditioning and propofol combined with sevoflurane anesthesia

Sponsors

Yongchuan Hospital Affiliated to Chongqing Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Subjects with ASA grade II to III; 2. Subjects aged 50-75 years old weighing 55-75kg; 3. Subjects of NYHA grade II to III.

Exclusion criteria

Exclusion criteria: 1. Subjects with ECG showing heart block; 2. Subjects with preoperative left ventricular ejection fraction (LVEF) < 40%; 3. Subjects with incomplete limbs had myocardial infarction in the past three months; 4. Patients with history of nervous system, immune system and mental diseases; 5. Subjects who used cardiotonics or needed mechanical assistance for heart failure before operation, those who had important organ diseases or underwent surgical treatment; 6. Subjects who used drugs that can improve myocardial blood supply and dilate cardiovascular system before operation; 7. Patients participating in other clinical trials.

Design outcomes

Primary

MeasureTime frame
blood pressure;heart rate;SPO2%;Blood gas analysis;Central venous pressure;H-FABP;cTnI;TNF-a;IL-8;

Secondary

MeasureTime frame
BIS value;Anesthetics dosage;The anesthesia time;The operation time;Age, gender, BMI;Adverse reactions;Hospital costs;Hospital costs;

Countries

China

Contacts

Public ContactChun Tian

Yongchuan Hospital Affiliated to Chongqing Medical University

272605765@qq.com+86 15723059158

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 10, 2026