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The efficacy of Desmopressin Acetate in reduction of post kidney biopsy bleeding among renal insufficiency patients: A randomized controlled trial.

Phase 4
Recruiting
Conditions
The patient with serum creatinine 1.5&#45
4 mg/dL who undergo native kidney biopsy.
kidney biopsy&#44
complication&#44
uremic bleeding&#44
desmopressin&#44
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
Inclusion Criteria

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

Exclusion Criteria

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
NameTimeMethod
Minor bleeding complication: bleeding without blood transfusion nor intervention 6 hours&#44; 24 hours after intervention hemoglobin&#44; hematoma size by ultrasound,Major bleeding complication: bleeding with requirement of blood transfusion or intervention 6 hours&#44; 24 hours after intervention hemoglobin&#44; hematoma size by ultrasound&#44; blood transfusion&#44; angiogram with embolization
Secondary Outcome Measures
NameTimeMethod
hematoma size between 2 groups 6 hours ultrasound,the different between vWF Ag&#44; RCO&#44; CBA level between 2 groups 1 hour after DDAVP injection measurement of vWF Ag&#44; RCO&#44; 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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