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      "title": "Two Different Regimens of Bemiparin as a Thromboprophylaxis in Morbidly Obese Surgical Patients",
      "scientificTitle": "Comparison of Two Different Regimens of Bemiparin as a Thromboprophylaxis After Surgery in Morbidly Obese Patients: A Randomized, Outcome-assessor Blinded Trial.",
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          "name": "Bemiparin 3500",
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          "description": "Bemiparin sodium 3,500 IU anti Xa/0.2 ml solution for injection in the pre-filled syringe will be provided for each patient in one group; subcutaneously 6 hours after the surgery(orthopedic and non-orthopedic) and then daily for up to 10 days for moderate and high - risk group and for 30 days in very high risk-group patients according to Caprinin risk classification for venous thromboembolism.\n\nOther Name: Hibor; Laboratories Rovi Pharmaceuticals"
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          "country": "Iraq",
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        "criteria": "Inclusion Criteria:\n\n1. Participants required surgical intervention in: general surgery, gynecology, bariatric surgery\n2. Moderate, high, and very high risk for venous thromboembolism according to Caprin RAM\n3. Participant is willing and able to give informed consent for participation in the study.\n4. BMI ≥40kg/m2\n\nExclusion Criteria:\n\n1. Having any contraindication to LMWH, such as active bleeding, history of heparin-induced thrombocytopenia , baseline platelet count \\<75 × 108/μl, severe renal disease (glomerular filtration rate \\<30 ml/minute), severe liver disease, or uncontrolled hypertension (\\>200/120 mmHg)\n2. Known hypersensitivity to unfractionated or LMWHs\n3. On oral or parenteral anticoagulants within 5 days before surgery\n4. Severe arterial hypertension\n5. Unable to comply with the study treatment and/or follow-up\n6. Receiving prohibited medications\n7. Pregnancy or lactation mother",
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