Safety Outcomes Post Kidney Biopsy - Randomized Clinical Evaluation of Efficacy of Desmopressin (STOP-BLEED)

Medical University of Bialystok

Status and phase: Enrolling; Phase 3

Conditions: Kidney Biopsy

Treatments: Drug: Desmopressin; Drug: intravenous infusion NaCl

Study type: Interventional

Funder types: Other

Identifiers

NCT05467033

2021/ABM/01/00100

Details and patient eligibility

About

It is a randomized, multicenter, double-blind, placebo controlled, interventional clinical trial that will be conducted in Poland, in about 6 Hospital Nephrology Departments to evaluate the safety and effectiveness of desmopressin on the prevention of bleeding after percutaneous needle kidney biopsy in patients with rare and ultrarare glomerulonephritis.

Full description

Glomerulonephritis (GN) are rare diseases which carry a high risk of morbidity and mortality. Very often it is diagnosed in the late stage of a disease. One of the reasons might be the fact of a concern for potential complications which might arise from kidney biopsy which is the only procedure which can confirm a diagnosis of glomerulonephritis. According to the map of health needs for Poland the estimated incidence of glomerulonephritis is 40.6 thousand people per year and approximately 1,250 percutaneous renal biopsy (PRB) are performed annually in the adult population.

There are few other studies which analyse the effect of DDAVP administration on the incidence of post-biopsy bleeding events in patients undergoing ultrasound guided PRB without previous coagulopathy. However, there were controversies regarding the potential side effects of DDAVP22 as the studies included only native kidneys biopsies Therefore, a clinical trial is planned with an adequately statistically powered sample of high-risk patients is planned Patients above 18 years old, already qualified by a nephrologist for a kidney biopsy will be randomized with random permuted blocks method into two equal groups (212 patients each) - in one 0,3 micrograms/kg i.v. of desmopressin (in 100 ml of 0,9% NaCl) will be administered one hour before procedure, in the second placebo only (100 ml of 0,9% NaCl). Kidney biopsy will be performed according to standard procedures by an experienced nephrologist with the use of 16G needles during a standard hospitalization with 48 hours of observation. The investigators will assess minor and major bleeding events occurring in the first 24 hours after the procedure (minor: macroscopic haematuria, clinically silent hematoma on kidney ultrasound performed 24 hours after the procedure, haemoglobin decrease above 20% from baseline; major: blood transfusion, embolization, nephrectomy, death indirectly or directly caused by the procedure) and for safety reasons the occurrence of hyponatremia 24 and 48 hours after kidney biopsy

Enrollment: 424 estimated patients

Sex: All

Ages: 18 to 99 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

1. ≥ 18 years old
2. Ability to provide Informed Consent
3. Qualification by nephrologist to kidney biopsy in accordance to current standards
4. Initial haemoglobin concentration > 8g/dl and PLT count >100 x103/μL
5. Normal range of APTT and INR
6. Blood pressure control defined as SBP<160 mmHg
7. Permitted antiplatelet/antithrombotic drugs: acetylsalicylic acid and heparin
8. No inflammation at the point of biopsy needle insertion

Exclusion criteria

1. Initial sodium concentration <130mmol/l

2. Pregnancy and breastfeeding

3. Anaphylactic shock after desmopressin administration (medical history)

4. Necessity of administration other anti-platelet / anti thrombotic drugs other than acetylsalicylic acid, non-fractionated heparin or low molecular weight heparin

5. Decompensated Heart failure

6. Von Willebrand disease (VWD) type II B

7. As per Investigator opinion a medical situation which may lead to increased intracranial pressure (ICP)

8. Hydronephrosis of the biopsied kidney

9. Usage of any prohibited drug before screening :

   • ASA in dosage > 75mg per day
   • Vitamin K antagonist (VKA)
   • Direct oral anticoagulants (DOAC)
   • Low-molecular-weight heparin (LMWH)
   • Unfractionated heparin (UFH)
   • Except situation when dosage of listed above drugs will be adjusted in accordance to protocol

Trial design

Primary purpose: Prevention

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Triple Blind

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424 participants in 2 patient groups, including a placebo group

Experimental

Experimental group

Description:

0,3ug/kg in 100ml 0,9% NaCl managed as intravenous infusion;

Treatment:

Drug: intravenous infusion NaCl

Drug: Desmopressin

Placebo comparator

Placebo Comparator group

Description:

0,9% NaCl managed as intravenous infusion;

Treatment:

Drug: intravenous infusion NaCl