To collect data on safety and effectiveness of dalteparin in the management of non-ST segment elevated acute coronary syndromes in nursing home patients who will be treated conservatively (without percutaneous corornary intervention \[PCI\] or coronary artery bypass graft \[CABG\] within 48 hours).
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Study Type
OBSERVATIONAL
Enrollment
618
Patients prescribed dalteparin for non-ST segment elevated acute coronary syndromes in nursing home patients who will be treated conservatively (without corornary intervention \[PCI\] or coronary artery bypass graft \[CABG\] within 48 hours).
Pfizer Investigational Site
Ahmedabad, Gujarat, India
Number of Participants With Death or Myocardial Infarction (MI)
Time frame: Baseline to 28 days after last dose of study drug
Number of Participants With Major Bleeding Events
Bleeding events were considered major if, accompanied by a decrease in hemoglobin of more than or equal to 2 grams/deciliter (g/dL) in connection with clinical symptoms; a transfusion was required; bleeding led to interruption of treatment or death; or intracranial bleeding.
Time frame: Baseline to 28 days after last dose of study drug
Number of Participants With Minor Bleeding Events
Bleeding events like hematuria, wound hematoma or injection site hematoma which did not fulfill the criteria for a major bleeding episode were classified as minor bleeding.
Time frame: Baseline to 28 days after last dose of study drug
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Pfizer Investigational Site
Surat, Gujarat, India
Pfizer Investigational Site
Hisar, Haryana, India
Pfizer Investigational Site
Hisar, Haryana, India
Pfizer Investigational Site
Bangalore, Karnataka, India
Pfizer Investigational Site
Manglore, Karnataka, India
Pfizer Investigational Site
Mysore, Karnataka, India
Pfizer Investigational Site
Nagpur, Maharahtra, India
Pfizer Investigational Site
Nashik, Maharahtra, India
Pfizer Investigational Site
Ambernath (E), Maharashtra, India
...and 14 more locations