The efficacy of Desmopressin Acetate in reduction of post kidney biopsy bleeding among renal insufficiency patients: A randomized controlled trial.
- Conditions
- The patient with serum creatinine 1.5dž mg/dL who undergo native kidney biopsy.kidney biopsy,complication,uremic bleeding,desmopressin,renal insufficiency
- Registration Number
- TCTR20150203001
- Lead Sponsor
- Siriraj Institutional Review Board Certificate of Approval
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 154
1. Age >/= 18 years old
2. Native kidney
3. Creatinine >/= 1.5 to < 4 mg/dL
4. BP < 160/80 mmHg before kidney biopsy
5. Normal platelet count and coagulogram
1. Single kidney
2. Kidney cancer
3. Hydronephrosis or pyelonephritis
4. BMI > 35 kg/m2
5. Dialysis free time < 2 weeks in case indicated dialysis
6. Different kidney size more than 2 cm.
7. The patient who takes antiplatelets or anticoagulants
8. Allergy to DDAVP
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Minor bleeding complication: bleeding without blood transfusion nor intervention 6 hours, 24 hours after intervention hemoglobin, hematoma size by ultrasound,Major bleeding complication: bleeding with requirement of blood transfusion or intervention 6 hours, 24 hours after intervention hemoglobin, hematoma size by ultrasound, blood transfusion, angiogram with embolization
- Secondary Outcome Measures
Name Time Method hematoma size between 2 groups 6 hours ultrasound,the different between vWF Ag, RCO, CBA level between 2 groups 1 hour after DDAVP injection measurement of vWF Ag, RCO, CBA level,the different between platelet aggregation test between 2 groups 1 hour after DDAVP injection platelet aggregation test,side effect of DDAVP 6 hours after DDAVP injection plasma sodium
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