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Alfalfa APP in the Medication Management of Anticoagulant therapy for patients

Alfalfa APP in the Medication Management of Anticoagulant therapy for patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500111022
Enrollment
Unknown
Registered
2025-10-23
Start date
2025-10-27
Completion date
Unknown
Last updated
2025-10-27

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

Conditions

Venous thromboembolism

Interventions

Pharmacist intervention group:On the basis of standard nursing care, the anticoagulant medication management for patients was carried out through the online platform of the Alfalfa APP
Standard Nursing Group:Anticoagulant medication management was carried out for patients through routine standard care

Sponsors

Fujian Maternity and Child Health Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1: Age >= 18 years old. 2: Suspected or diagnosed as malignant tumors of the female reproductive organs, not specifically specified. 3: Gynecological malignant tumor surgery is planned to be performed during the hospitalization. 4: Anticoagulant therapy lasts for at least 28 days. 5: Receive anticoagulant drug management through the Alfalfa APP or regular standard care. 6: The patient has no communication and interaction barriers and can cooperate with regular follow-up examinations as required. 7: Agree to participate in this study and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1: The hospital's electronic medical record system retrieves information related to cognitive impairment or mental disorders. 2: Severe liver dysfunction (total bilirubin higher than twice the upper limit of normal, and AST/ALT/ALP higher than three times the upper limit of normal). 3: Severe renal insufficiency (endogenous creatinine clearance rate =30mL/min). 4: People with thrombotic diseases. 5: Long-term use of non-steroidal anti-inflammatory drugs. 6: Patients diagnosed with benign gynecological tumors during the operation. 7: Pregnancy or breastfeeding. 8: Patients with contraindications to anticoagulation (with risks of active bleeding, liver failure, blood diseases or contraindicated bleeding, and contraindications to the use of anticoagulants). 9: Uncontrolled severe hypertension (systolic blood pressure >200 mm Hg or diastolic blood pressure >120 mm Hg). 10: One of the following uncontrolled or unstable cardiovascular diseases exists: stroke, acute ischemia or myocardial infarction confirmed by electrocardiogram, and/or clinically significant arrhythmia. 11: Use artificial heart valves. 12: The physician believes that participating in the trial is not in the best interests of the patients.

Design outcomes

Primary

MeasureTime frame
Anticoagulation cognitive questionnaire score;

Secondary

MeasureTime frame
Venous thromboembolism;Medication satisfaction;Medication compliance;

Countries

China

Contacts

Public ContactTing Wei

Fujian Maternity and Child Health Hospital

weiting6012@fjsfy.com+86 189 0691 8492

Outcome results

None listed

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