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Parham Sadeghipour

Researcher at Iran University of Medical Sciences

Publications -  87
Citations -  1204

Parham Sadeghipour is an academic researcher from Iran University of Medical Sciences. The author has contributed to research in topics: Medicine & Internal medicine. The author has an hindex of 10, co-authored 59 publications receiving 483 citations. Previous affiliations of Parham Sadeghipour include Tehran University of Medical Sciences & Iran University of Science and Technology.

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Effect of Intermediate-Dose vs Standard-Dose Prophylactic Anticoagulation on Thrombotic Events, Extracorporeal Membrane Oxygenation Treatment, or Mortality Among Patients With COVID-19 Admitted to the Intensive Care Unit: The INSPIRATION Randomized Clinical Trial.

Inspiration Investigators, +63 more
- 27 Apr 2021 - 
TL;DR: In this paper, the authors evaluated the effects of intermediate-dose vs standard-dose prophylactic anticoagulation among patients with COVID-19 admitted to the intensive care unit (ICU).
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Antibiotics for treating human brucellosis

TL;DR: The pooled analysis did not demonstrate any significant difference between two regimens in terms of relapse and symptom persistence, but showed a non-significant higher risk of minor adverse reactions in doxycycline plus rifampicin (RR 1.80, 95% CI 0.99 to 1.92).
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International Prospective Registry of Acute Coronary Syndromes in Patients With COVID-19.

TL;DR: In this article, the authors report the demographics, angiographic findings, and in-hospital outcomes of COVID-19 patients and compare these with pre-COVID19 cohorts.
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Intermediate versus standard-dose prophylactic anticoagulation and statin therapy versus placebo in critically-ill patients with COVID-19: Rationale and design of the INSPIRATION/INSPIRATION-S studies.

TL;DR: INSPIRATION and INSPIRATON-S studies will help address clinically-relevant questions for antithrombotic therapy and thromboinflammatory therapy in critically-ill patients with COVID-19 and test two independent hypotheses within a randomized control trial with 2 × 2 factorial design.