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Effects of remote ischemic preconditioning on the incidence of postoperative atrial fibrillation in middle and young patients undergoing cardiac valve surgery : a single-center, prospective study

Effects of remote ischemic preconditioning on the incidence of postoperative atrial fibrillation in middle and young patients undergoing cardiac valve surgery : a single-center, prospective study

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400087721
Enrollment
Unknown
Registered
2024-08-02
Start date
2024-03-17
Completion date
Unknown
Last updated
2024-08-05

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

Conditions

postoperative atrial fibrillation after cardiac valve surgery

Interventions

remote ischemic preconditioning group:In the remote ischemic preconditioning group, the patient was treated with ischemia and reperfusion 18 h before surgery, inflated with the right upper limb cuff t
control group:The control group do not undergo distal ischemic preconditioning.

Sponsors

General Hospital of Northern Theater Command
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 64 Years

Inclusion criteria

Inclusion criteria: 1.Age: 18 years= Age <65 years; 2.The following procedures were performed at elective times: cardiac valve surgery (without CABG).

Exclusion criteria

Exclusion criteria: 1.Patients with preoperative atrial fibrillation; 2.Not agree to participate in the investigator; 3.Patients cannot cooperate and cannot complete the follow-up requirements as required; 4.Patients are participating in other clinical trials; 5.Patients that other investigators consider are not fit to participate; 6.Patients undergoing a second or more thoracotomy procedure; 7.Patients with severe cardiac, hepatic and renal dysfunction; 8.The anterior and posterior diameter of the left atrium is greater than or equal to 60mm; 9.Condication to remote ischemia adaptation, such as more severe soft tissue injury, fracture or vascular injury, and peripheral vascular lesions of the distal upper limb, etc.

Design outcomes

Primary

MeasureTime frame
postoperative atrial fibrillation;

Secondary

MeasureTime frame
Postoperative complications;Postoperative hospitalization time;Atrial fibrillation burden of postoperative new onset atrial fibrillation;

Countries

China

Contacts

Public ContactHan Jinsong

General Hospital of Northern Theater Command

hanjs0216@sina.com+86 133 5245 6086

Outcome results

None listed

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