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Efficacy of Regional Citrate Anticoagulation versus SalineFlushingduring Intermittent Hemodialysis on blood circuit clotting prevention;A Randomized Clinical Trial

Phase 3
Conditions
hypocalcemia hypernatremia metabolic alkalosis cardiac arrhythmia
Regional citrate anticoagulants Saline flushing intermittent hemodialysis
Registration Number
TCTR20210929007
Lead Sponsor
Bhumibol Adulyadej Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending (Not yet recruiting)
Sex
All
Target Recruitment
42
Inclusion Criteria

Acute setting ; AKI,ESRD Age > 18 yrs Informed consent Undergoing central venous catheters or AVF/AVG, by prescription HD: Low flux dialyzer BFR 200 ml/min Dialyzate Ca 1.75 mEq/L Duration 4 hr

Exclusion Criteria

1.Patients were treated with antiplatelet,oral anticoagulant therapy or other drugs known to affect coagulation within 7 days 2. Acute liver failure 3. DIC 4. Contraindication to systemic anticoagulation: Abnormal plasma total calcium < 7.0 mg/dL Abnormal plasma total magnesium <1.8 mg/dL Abnormal plasma total sodium >145 mg/dL metabolic alkalosis; serum bicarb > 28 mEq/L Known allergy to citrate Documented arrhythmia

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Dialyzer clots 0,60,120,240 min percent of dialyzer clots
Secondary Outcome Measures
NameTimeMethod
hypocalcemia 0,60,120,240 min incidence of hypocalcemia,hypernatremia 0,60,120,240 min incidence of hypernatremia,metabolic alkalosis 0,60,120,240 min incidence of metabolic alkalosis
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