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NCT07243704From ClinicalTrials.govRecruiting

Reducing the Burden of Cardiovascular Events With Antiplatelet Therapy in Patients With IntraCerebral Haemorrhage

Reducing the Burden of Cardiovascular Events With Antiplatelet Therapy in Patients With IntraCerebral Haemorrhage.

  • Intracerebral Haemorrhage

At a glance

Phase
Phase 3
Study type
Interventional
Sponsor
Christian Medical College and Hospital, Ludhiana, India
Enrolment target
5,676
Started
16 February 2026
Main results due
15 February 2029
Study sites
33
Registry updated
24 September 2026

Can you take part?

  • Ages 18 years to 99 years.
  • Open to any sex.
  • You need the condition being studied — healthy volunteers are not accepted.

These are the headline rules only. Every study has a longer list, and whether you are eligible is decided by the research team at the site — never by this page.

Read the full eligibility criteria
Inclusion Criteria:

* Age ≥18 years
* First-ever Intracerebral Haemorrhage
* Presenting ≥24 hrs up to 3 months of stroke symptoms confirmed by brain imaging
* CT /MRI confirming Intracerebral Haemorrhage
* Alive ≥24 hours after non-traumatic ICH

Exclusion Criteria:

* ICH is known to be due to trauma, a structural cause (e.g., aneurysm, arteriovenous malformation, cerebral cavernous malformation, venous thrombosis, or tumour), or haemorrhagic transformation of cerebral infarction
* Glasgow coma score ≤5
* Taking any antiplatelet or anticoagulant therapy 15 days prior to randomization.
* Women pregnant, breastfeeding, childbearing potential, and not using contraceptives
* Enrolled in any other clinical trial
* Sick or compromised patients with life expectancy of less than a year
* Geographical or other factors that prohibit long-term follow-up

What this study is about

In the sponsor’s own words, from the registry.

BEAT ICH will be a pragmatic, randomised, placebo-controlled, blinded, superiority clinical trial aiming to recruit 5676 patients aged ≥18 years who survive ICH and assign them 1:1 to starting antiplatelet monotherapy (Aspirin 75 mg od) versus placebo for the entire duration of the trial for preventing MACE. Recruitment duration is for 2.5 years. The duration of the medication and follow-up will vary based on recruitment timeline. If recruited during the first year of the trial, the patient will take the medication for three years or until the trial ends or an event occurs, with a matching follow-up period. If recruited towards the end of the trial, he/she will take the medication for six months and be followed up for the same duration. The trial's follow-up duration is three years. The patients will be recruited for 2.5 years, and the last recruit will have a minimum follow-up of six months. No new patients will be recruited within the last six months of the trial, but all the patients will be followed up until the end of the trial.

Study sites(33)

  • Government General Hospital

    Guntur, Andhra Pradesh, India

    Recruiting

  • Lalitha Super Specialty Hospital

    Guntur, Andhra Pradesh, India

    Recruiting

  • Dr Ramesh Cardiac and Multispecialty Hospital

    Guntur, Andhra Pradesh, India

    Recruiting

  • Government General Hospital

    Kākināda, Andhra Pradesh, India

    Recruiting

  • Narayana Medical College and Hospital

    Nellore, Andhra Pradesh, India

    Recruiting

  • Apollo Excelcare Hospitals

    Guwahati, Assam, India

    Recruiting

  • Baptist Christian Hospital

    Tezpur, Assam, India

    Recruiting

  • All India Institute of Medical Science

    Patna, Bihar, India

    Recruiting

  • Rajendra Institute of Medical Sciences

    Ranchi, Jharkhand, India

    Recruiting

  • KLE's Dr. Prabhakar Kore Hospital & Medical Research Centre

    Belagavi, Karnataka, India

    Recruiting

  • Amrita Institute for Medical Sciences and Research Center

    Kochi, Kerala, India

    Recruiting

  • Government Medical College Trivandrum

    Thiruvananthapuram, Kerala, India

    Recruiting

  • Sree Chitra Tirunal Institute for Medical Sciences and Technology

    Thiruvananthapuram, Kerala, India

    Recruiting

  • P. D. Hinduja Hospital and Medical Research Centre

    Mumbai, Maharashtra, India

    Recruiting

  • Bharati Vidyapeeth DTU Medical College

    Pune, Maharashtra, India

    Recruiting

  • Institute of Human Behaviour and Allied Sciences

    New Delhi, National Capital Territory of Delhi, India

    Recruiting

  • All India Institute of Medical Sciences

    Bhubaneswar, Odisha, India

    Recruiting

  • Guru Gobind Singh Medical College and Hospital

    Farīdkot, Punjab, India

    Recruiting

  • PBM Hospital

    Bikaner, Rajasthan, India

    Recruiting

  • Santokba Durlabhji Memorial Hospital

    Jaipur, Rajasthan, India

    Recruiting

  • Jaiswal Hospital and Neuro Institute

    Kota, Rajasthan, India

    Recruiting

  • KG Hospital and Post Graduate Medical Institute Coimbatore

    Coimbatore, Tamil Nadu, India

    Recruiting

  • Christian Medical College Vellore

    Vellore, Tamil Nadu, India

    Recruiting

  • King George's Medical University

    Lucknow, Uttar Pradesh, India

    Recruiting

  • All India Institute of Medical Sciences

    Raebareli, Uttar Pradesh, India

    Recruiting

  • Institute of Medical Sciences of the Banaras Hindu University (BHU)

    Varanasi, Uttar Pradesh, India

    Recruiting

  • Bangur Institute of Neurosciences

    Kolkata, West Bengal, India

    Recruiting

  • St Stephen's Hospital

    Delhi, India

    Recruiting

  • All India Institute of Medical Science

    Guwahati, India

    Recruiting

  • KIMS-Sunshine Hospitals

    Hyderabad, India

    Recruiting

  • Renova Institute of Neurological Sciences (RINS); Renova Century Hospital

    Hyderabad, India

    Recruiting

  • Sanjay Gandhi Postgraduate Institute of Medical Sciences

    Lucknow, India

    Recruiting

  • All India Institute of Medical Science

    New Delhi, India

    Recruiting

Showing 33 of 33 sites. 33 of the 33 sites on this study are recruiting right now — a site can stop enrolling while the study as a whole is still open.

Source: ClinicalTrials.gov record NCT07243704. Trialion does not run this study, is not paid to refer anyone to it, and cannot enrol you. Eligibility is always decided by the research team at the site.

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Reducing the Burden of Cardiovascular Events With Antiplatelet Therapy in Patients With IntraCerebral Haemorrh | Trialion