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NCT Number: NCT05848713

AntiThrombotic Therapy to Ameliorate Clinical Complications in Community Acquired Pneumonia

This is an international, open-label, stratified randomized controlled trial with Bayesian adaptive stopping rules to compare the effects of therapeutic-dose heparin vs. usual care pharmacological thromboprophylaxis on outcomes in patients admitted to hospital with community acquired pneumonia (CAP).

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

Hospital Estadual Dr. Jayme Santos Neves, Serra, Espírito Santo, Brazil

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About this study

The global incidence of hospitalization due to CAP is high and associated with substantive morbidity and mortality. Thrombotic complications - including venous, arterial, and possibly microvascular - occur commonly in hospitalized patients across many etiologies of CAP. Poor outcomes may be mediated by both inflammatory and thrombotic processes leading to respiratory, cardiac, and other end organ dysfunction. There are currently no established therapies that modify the potentially maladaptive immunothrombosis pathway in CAP.

Therapeutic-dose anticoagulation with heparin reduces disease progression and mortality in non-critically ill patients hospitalized with COVID-19 with an acceptable safety profile. COVID-19 shares pathogenic features, including activation of the inflammatory and coagulation cascades, with other pneumonias. Whether therapeutic-dose heparin confers similar clinical benefits in non-COVID-19 CAP is unknown.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients ≥18 years of age
  • Admitted to hospital for a suspected or confirmed diagnosis of CAP defined by:
  • Radiographic evidence of new or worsening infiltrate
  • One or more of the following signs and/or symptoms of lower respiratory tract infection

i. New or increased cough or sputum production ii. Fever of > 37.8C or temperature < 36C iii. WBC > 11 x 109/L or < 4 x 109/L c. The primary diagnosis is believed to be CAP as per the attending physician

  • Requires supplemental oxygen to treat hypoxemia (or requires an increased level of supplemental oxygen if on chronic oxygen therapy)
  • Hospital admission anticipated to last ≥72 hours from randomization

Exclusion criteria

  • Suspected or confirmed active COVID-19 infection
  • Hospital admission for >72 hours prior to randomization
  • Patients receiving non-invasive or invasive ventilation, vasopressors, or extracorporeal life support (ECLS) within an ICU at the time of enrollment
  • Requirement for chronic mechanical ventilation via tracheostomy prior to hospitalization
  • Patients for whom the intent is to not use pharmacologic thromboprophylaxis
  • Patients with an independent indication for therapeutic-dose anticoagulation
  • Patients with a contraindication to therapeutic-dose anticoagulation, including:
  • Non-traumatic bleeding that requires medical evaluation or hospitalization within 30 days prior to CAP hospital admission
  • History of an inherited or acquired bleeding disorder
  • Cerebral aneurysm or mass lesions of the central nervous system
  • Ischemic stroke within 3 months of hospital admission
  • Gastrointestinal bleeding within 3 months of hospital admission
  • Platelet count <50 x109/L OR INR >2.0 OR hemoglobin <80 g/L at the time of screening
  • Other physician-perceived contraindications to therapeutic anticoagulation
  • History of heparin induced thrombocytopenia (HIT) or other heparin allergy
  • Current or recent (within 7 days of screening) use of dual anti-platelet inhibitors (For example; Aspirin + one of the following; clopidogrel, ticagrelor, prasugrel)
  • Patients in whom imminent death is anticipated
  • Anticipated transfer to another hospital that is not a study site within 72 hours of randomization
  • Enrollment in other interventional trials related to anticoagulation or antiplatelet therapy during current hospitalization

Treatment and study plan

Heparin

Drug

Preference is for LMWH given ease of administration and possibility of a more favorable safety profile, if no contraindication is present. Enoxaparin, dalteparin, or tinzaparin are acceptable LMWHs to be used for patients in the investigational arm and dose should be based on measured or estimated weight of the patient.

Alternatively, intravenous UFH may be used and may be preferred in the presence of significant renal compromise. Intravenous UFH is typically dosed according to total body weight and pragmatically adjusted according to local institutional policy to achieve an activated partial thromboplastin time (aPTT) of 1.5-2.5x the reference value, or a corresponding UFH anti-Xa level. If UFH is used, the availability of a local site policy that specifies an aPTT target in this range or a corresponding anti-Xa value is a requirement.

Primary outcomes

  1. Ordinal endpoint reflecting survival

    Time frame: 30 days

    Survival to hospital discharge without ICU-level organ support. Organ support is defined as receipt of high flow nasal oxygen, invasive or non-invasive mechanical ventilation, vasopressor/inotropic therapy, or extracorporeal life support (ECLS) within an ICU. This outcome reflects disease progression to ICU-level organ failure or the worst possible outcome (death). It was chosen because of its importance to patients, clinicians, and other stakeholders. Given the limited number of ICU beds, reducing the burden of critical illness has important health system capacity implications.

Secondary outcomes

  1. Bleeding events

    Time frame: 14 days

    Number of participants with major bleeds as defined by the ISTH definition.

  2. HIT events

    Time frame: 14 days

    Number of participants with laboratory confirmed heparin induced thrombocytopenia (HIT)

  3. Thrombotic events

    Time frame: 30 days and 90 days

    Number of participants with deep vein thrombosis, pulmonary embolism, systemic arterial thromboembolism, myocardial infarction, or ischemic stroke

  4. Invasive mechanical ventilation

    Time frame: 30 days

    Ordered categorical endpoint with three possible outcomes based on the worst status of each patient through day 30 following randomization

  5. All cause mortality

    Time frame: 30 days, 90 days, and 180 days

  6. Hospital-free days

    Time frame: 30 days, 90 days, and 180 days

    Days alive outside hospital

  7. Health related quality of life

    Time frame: 30 days, 90 days, and 180 days

    Using the EQ-5D-5L instrument

  8. Health related quality of life

    Time frame: 30 days, 90 days, and 180 days

    Using the Clinical Frailty Scale instrument

Study contacts

Contact information is provided by the study sponsor or research team.

Chantale Pineau

CONTACT

[email protected]

2042353223

Sponsors and collaborators

Lead sponsor

University of Manitoba

Other

Collaborators

  • Aurora Clinical Research
  • Avanti PC
  • Canadian Critical Care Trials Group
  • Canadian Institutes of Health Research (CIHR)
  • Canadian Venous Thromboembolism Clinical Trials and Outcomes Research (CanVECTOR) Network
  • Ozmosis Research Inc.
  • Research Manitoba

Registry information

Acronym: ATTACC-CAP

Important dates

Study start
2023
Primary completion
2028
Study completion
2029
First posted
May 8, 2023
Registry last updated
Apr 21, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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