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Effect of standard perioperative management on the incidence of perioperative comprehensive complications in patients with chronic anticoagulation: a prospective study

Effect of standard perioperative management on the incidence of perioperative comprehensive complications in patients with chronic anticoagulation: a prospective study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100043626
Enrollment
Unknown
Registered
2021-02-23
Start date
2021-03-01
Completion date
Unknown
Last updated
2021-06-22

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

Conditions

Perioperative management of antithrombotic medication

Interventions

Intervention group :standard perioperative management
Controlled group :routine perioperative management

Sponsors

Peking University First Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.Patients who have long-term use of antithrombotic drugs for cardiovascular and cerebrovascular diseases, including antiplatelet drugs and/or anticoagulant drugs (such as aspirin, clopidogrel, ticagrelor, warfarin, dabigatran, rivaroxaban, etc.). Long-term use refers to taking above drugs continuously for more than 2 weeks and is still taking them within 1 month before admission. 2.Patients who have one or more of the following situations: (1) Non-valvular atrial fibrillation with CHA2DS2-VASc score above 4; (2) Post- artificial valve replacement(including mitral valve, ball-cage valve or tilting disc aortic valve); (3) Venous thromboembolism occurred within 1 year, or venous thromboembolism with other high-risk factors which requires long-term anticoagulation treatment;(4)Coronary heart disease with coronary stent implantation, thrombolytic therapy or other coronary procedures within 2 years, or who had undergone coronary artery bypass grafting within 1 year, or who experienced myocardial infarction or acute coronary syndrome within 1 year; (5) A history of stroke/TIA within 1 year, or a history of cervical or intracranial revascularization treatment within 1 year; (6) Peripheral arterial disease. 3.Patients who will undergo abdominal surgery (including general and urologic surgery); 4.Patients who signed informed consent form.

Exclusion criteria

Exclusion criteria: 1. Refuse to participate; 2. Emergency surgery; 3. Unable to complete the preoperative assessment and follow-up plan; 4. There are other reasons which researcher/attending doctor think that the patient is not suitable for the trial.

Design outcomes

Primary

MeasureTime frame
The incidence of bleeding events and major adverse cardiovascular or cerebrovascular events during perioperative period;

Secondary

MeasureTime frame
The incidence of overall complications during perioperative period;The length of hospital stay;hospitalization expenses;All-cause mortality rate within 30 days after surgery;

Countries

China

Contacts

Public ContactHong Zhang

Peking University First Hospital

zhanghong40@hotmail.com+86 13910104660

Outcome results

None listed

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