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Apixaban in heparin-induced thrombocytopenia

Evaluation of the efficacy of apixaban in the treatment of heparin-induced thrombocytopenia (HIT)

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200325046854N1
Enrollment
30
Registered
2021-04-25
Start date
2021-05-22
Completion date
Unknown
Last updated
2021-05-26

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

Conditions

Heparin-induced thrombocytopenia. Thrombocytopenia, unspecified

Interventions

Intervention group: In patients admitted to the internal ward of Rasool Akram Hospital who are diagnosed with HIT by the 4T Score, heparin will be discontinued and apixaban will be started. Based on
so we will use mentioned dose in the treatment of DVT or PE and in the prevention of stroke in non-valvular ?AF. In prophylactic setting, we will use a dose of 2.5 mg twice a day, unless the patient e

Sponsors

Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1) Age 18 years or older 2) HIT detection based on 4T Score equal to or above 4

Exclusion criteria

Exclusion criteria: Patients with active bleeding Patient with inherited or acquired coagulation disease or bleeding disorder Patients receiving cytochrome P-450 3A4 inhibitors or inducers Severe renal failure (CrCl <25 ml / min) Severe liver disease (including Child-Pugh B and C) The patient needs surgery History of uncorrected cerebral aneurysm, intracranial tumor or vascular accident Non-participation in research projects during the 30 days prior to the study Pregnant and lactating women Previous treatment with a non-heparin anticoagulant Covid-19 infection

Design outcomes

Primary

MeasureTime frame
Follow-up of arterial / venous thrombosis after receiving apixaban. Timepoint: If the patient becomes symptomatic. Method of measurement: Doppler ultrasound.

Secondary

MeasureTime frame
Mortality rate. Timepoint: Daily. Method of measurement: Loss of vital signs and death of the patient.;Bleeding event following the use of apixaban. Timepoint: Daily. Method of measurement: Based on the patient's symptoms such as petechiae.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMaryam Farasatinasab

Iran University of Medical Sciences

maryfarasati@gmail.com+98 21 8214 1000

Outcome results

None listed

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