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The Effect of 6% Hydroxyethyl Starch 130/0.4 on Blood Loss and Coagulation in Patients Medicated With Antiplatelet Agents Prior to Off-Pump Coronary Bypass Graft Surgery

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Yonsei University

Status and phase

Completed
Phase 4

Conditions

Coronary Artery Occlusive Disease

Treatments

Drug: 6% hydroxyethyl Stach 130/0.4

Study type

Interventional

Funder types

Other

Identifiers

NCT01051206
4-2009-0057

Details and patient eligibility

About

HES 130/0.4 significantly solution will not affect on coagulation and blood loss in patients medicated with antiplatelet agents prior to off-pump coronary bypass surgery (OPCAB).

Enrollment

106 estimated patients

Sex

All

Ages

20+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Eighty patients undergoing OPCAB, who were exposed to anti platelet agents until 5 days prior to surgery were randomly allocated to infuse HES 130/0.4 up to 30 ml/kg and followed crystalloid infusion or infuse crystalloid only during perioperative period,

Exclusion criteria

Patient who has

  • Valvular disease of heart
  • MI within 3 months,patient under 40% of left ventricle preoperative output
  • left main artery stenosis
  • anemia (hemoglobin < 12 g/dl), coagulopathy (Platelet < 100/nl, activated partial thromboplastin time, aPTT) > 80sec, serum creatinine > 1.2 mg/dl, respiratory disease(asthma, COPD, PaO2 < 70 mmHg, pulmonary hypertension or pulmonary edema, etc)
  • not consented to this trial

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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