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A Study of Indobufen Combined with Ticagrelor for the Treatment of Acute Minor Stroke or TIA.

A Study of Indobufen Combined with Ticagrelor for the Treatment of Acute Minor Stroke or TIA. - ITAS

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400085456
Enrollment
Unknown
Registered
2024-06-07
Start date
2024-06-14
Completion date
Unknown
Last updated
2024-07-08

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

Conditions

Stroke

Interventions

1:Aspirin 100mg administered orally once daily, initiated within 72 hours of symptom onset, continued for 90 days, in conjunction with ticagrelor therapy (a loading dose of 180mg on the first day, fol
0:In patients within 72 hours of symptom onset, indobufen 100mg was administered orally twice daily for 90 days, coupled with ticagrelor therapy (commencing with a single loading dose of 180mg on the

Sponsors

The People's Hospital of Qiannan, Guizhou Province, China
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1.Age = 40 years; 2.Acute mild ischemic stroke (NIHSS score = 3 at randomization), with time from symptom onset to treatment initiation = 72 hours, or Transient Ischemic Attack (TIA) with an ABCD2 score = 4; 3.Provision of informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients with coagulation disorders, malignancies, hematological diseases, or severe hepatic or renal dysfunction. 2. Patients with intracranial hemorrhage diagnosed by head CT or MRI. 3. Patients with a prior definitive diagnosis of multiple sclerosis. 4. Patients with known allergies to aspirin, ticagrelor, or indobufen. 5. Patients with atrial fibrillation or other thromboembolic conditions requiring anticoagulation therapy. 6. Patients planning to undergo surgical procedures within 3 months necessitating medication discontinuation. 7. Patients with a platelet count below 100×109/L prior to randomization. 8. Patients who had gastrointestinal bleeding or underwent open surgery within 3 months preceding randomization. 9. Women of childbearing potential not using contraception, or patients with a positive pregnancy test. 10. Patients with severe cardiac or pulmonary dysfunction and a life expectancy of less than 3 months. 11. Patients concurrently participating in other clinical trials.

Design outcomes

Primary

MeasureTime frame
Recurrence of stroke;

Secondary

MeasureTime frame
Abdominal pain;Melena;Symptomatic intracranial hemorrhage ;intracranial hemorrhage;Cutaneous ecchymosis;Mortality within 90 days;

Countries

China

Contacts

Public ContactKaiwu Meng

Neurology Department, The people's hospital of QianNan, GuiZhou Province, People's Republic of China.

meng18684121778@163.com+86 186 8412 1778

Outcome results

None listed

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