search
Back to results

A Study on the Efficacy and Safety of Continuous Renal Replacement Therapy (CVVHDF) Using a Commercial Citrate-containing Replacement Fluid (Prismocitrate 18/0)

Primary Purpose

Renal Failure

Status
Completed
Phase
Not Applicable
Locations
Hong Kong
Study Type
Interventional
Intervention
Prismocitrate 18/0, Prism0cal
Sponsored by
The University of Hong Kong
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Renal Failure

Eligibility Criteria

18 Years - 90 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • The patient requires CRRT as treatment for renal failure, as decided by the attending physician
  • The patient fulfils at least one of the following clinical criteria for initiating CRRT:

    1. According to the RIFLE criteria, (11) patients satisfying the "injury" criteria (increase creatinine by 2 fold or urine output<0.5ml/kg/hr for 12hr) will be considered for CRRT
    2. Hyperkalemia ([K+] > 6.5 mmol/L).
    3. Severe acidemia (pH < 7.2).
    4. Urea > 25 mmol/liter.
    5. Clinically significant organ oedema in the setting of ARF.

      Exclusion Criteria:

Sites / Locations

  • Adult Intensive Care unit, Queen Mary Hospital

Arms of the Study

Arm 1

Arm Type

Other

Arm Label

Prismocitrate 18/0

Arm Description

citrate-containing replacement solution (Prismocitrate 18/0, Gambro) will be administered at pre-filter port during continuous hemodiafiltration, for the purpose as replacement solution and anticoagulation

Outcomes

Primary Outcome Measures

filter lifespan
filter lifespan will be recorded as the time duration from commencement of renal replacement therapy till filter clotted or therapy ended

Secondary Outcome Measures

metabolic and electrolyte control
Serum electrolytes (calcium, sodium, potassium, magnesium, acid-base)will be monitored at baseline, then every 6 hours onwards during the CRRT
bleeding/transfusion requirement
blood counts including the hemoglobin level and patient clinical status will be monitored at baseline, then once everyday during renal replacement therapy

Full Information

First Posted
July 31, 2013
Last Updated
December 2, 2014
Sponsor
The University of Hong Kong
search

1. Study Identification

Unique Protocol Identification Number
NCT01921816
Brief Title
A Study on the Efficacy and Safety of Continuous Renal Replacement Therapy (CVVHDF) Using a Commercial Citrate-containing Replacement Fluid (Prismocitrate 18/0)
Study Type
Interventional

2. Study Status

Record Verification Date
December 2014
Overall Recruitment Status
Completed
Study Start Date
May 2012 (undefined)
Primary Completion Date
August 2013 (Actual)
Study Completion Date
undefined (undefined)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
The University of Hong Kong

4. Oversight

5. Study Description

Brief Summary
The investigators aim to examine the efficacy and safety of using a new citrate containing commercially available solutions (Prismocitrate 18/0) as the regional citrate anticoagulation in continuous renal replacement therapy for critically ill patients.
Detailed Description
Acute kidney injury is common in critically ill patients, and continuous renal replacement therapy is the preferable mode of treatment to remove the metabolic waste while avoiding the hemodynamic instability associated with intermittent hemodialysis. Thrombosis frequently occurs in the hemofilter which could reduce the circuit lifespan, jeopardize the efficacy of renal replacement, result in loss of blood cells and increased transfusion requirement. Anticoagulants including conventional heparin and low molecular weight heparin, introduced via the arterial port of the circuit, are widely used to reduce clotting within the extracorporeal circuit. However, significant amount of heparin is not removed in the circuit and will be carried into patient's circulation, which could lead to bleeding complications. Regional citrate anticoagulation (RCA) has been used for intermittent haemodialysis since 1983, and its use has extended to that for continuous renal replacement therapy (CRRT) since 1987. Citrate is introduced at therapeutic level at the arterial limb of the dialysis circuit, where it chelates calcium ions in the blood to prevent clotting within the hemofilter. While some calcium-citrate complex is removed in the filter, the residual will be circulated to the patient and be metabolized in liver. Patient's systemic ionized calcium level remains normal, by hemodilution and also calcium replacement. Therefore, the anticoagulant effect from citrate is regional and confined to the extracorporeal circuit. RCA has the potential to extend circuit life during renal replacement therapy without systemic anticoagulation. In a recent meta-analysis of randomized controlled trials, RCA was as efficacious as heparin anticoagulation in term of maintaining circuit function, and RCA was associated with decreased risk of bleeding with no significant increase in incidence of metabolic alkalosis.(5) Hypocalcemia was more common in patients receiving citrate, but of note, no clinical adverse event was reported in the included studies. Although citrate anticoagulation had repeatedly been demonstrated to prolong filter life, many hospitals still refrained from using it, as a result of limited experience, different patient variety, or other reasons. The investigators' group has performed a pilot study (HKU/HA HKW IRB No: UW 08-221) to assess the efficacy and safety of continuous venous-venous hemodiafiltration(CVVHDF) using a commercial citrate containing replacement fluid (Prismocitrate 10/2, Gambro) which contains 10mmol/l citrate and 2 mmol/l citric acid. 15 subjects were recruited from July 2008 to June 2011. No serious adverse events were reported, including severe hypocalcemia, hypercalcemia, citrate toxicity and severe acid base disturbances. Metabolic acidosis due to renal failure were only partially corrected by CRRT with citrate anticoagulation in the initial study subjects, the problem was subsequently solved by adding supplemental bicarbonate to the dialysate. Since then, all the patients were able to complete the treatment protocols with adequate kidney lifespan, correction of metabolic abnormalities and fluid imbalance. However, since additional bicarbonate is needed to correct the metabolic acidosis during CRRT, there is room for improvement regarding the formulation of the citrate-containing solution to reduce acid liberation while increasing the alkali bicarbonate production. Prismocitrate 18/0, which contains 18mmol/l citrate (one mmol citrate could be metabolized to produce 3 mmol bicarbonate) and no citric acid, could potentially result in better acid-base control during CRRT.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Renal Failure

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
35 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Prismocitrate 18/0
Arm Type
Other
Arm Description
citrate-containing replacement solution (Prismocitrate 18/0, Gambro) will be administered at pre-filter port during continuous hemodiafiltration, for the purpose as replacement solution and anticoagulation
Intervention Type
Device
Intervention Name(s)
Prismocitrate 18/0, Prism0cal
Other Intervention Name(s)
Prismocitrate 18/0 (replacement solution), Prism0cal (dialysate), Gambro
Intervention Description
Subjects on continuous hemodiafiltration will ordinarily receive heparin as the anticoagulation. In our study, regional citrate anticoagulation with Prismacitrate is used to replace heparin. Citrate has been shown in study to be safer than heparin with reduced bleeding risk
Primary Outcome Measure Information:
Title
filter lifespan
Description
filter lifespan will be recorded as the time duration from commencement of renal replacement therapy till filter clotted or therapy ended
Time Frame
up to 4 days
Secondary Outcome Measure Information:
Title
metabolic and electrolyte control
Description
Serum electrolytes (calcium, sodium, potassium, magnesium, acid-base)will be monitored at baseline, then every 6 hours onwards during the CRRT
Time Frame
up to 4days
Title
bleeding/transfusion requirement
Description
blood counts including the hemoglobin level and patient clinical status will be monitored at baseline, then once everyday during renal replacement therapy
Time Frame
up to 4 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: The patient requires CRRT as treatment for renal failure, as decided by the attending physician The patient fulfils at least one of the following clinical criteria for initiating CRRT: According to the RIFLE criteria, (11) patients satisfying the "injury" criteria (increase creatinine by 2 fold or urine output<0.5ml/kg/hr for 12hr) will be considered for CRRT Hyperkalemia ([K+] > 6.5 mmol/L). Severe acidemia (pH < 7.2). Urea > 25 mmol/liter. Clinically significant organ oedema in the setting of ARF. Exclusion Criteria:
Facility Information:
Facility Name
Adult Intensive Care unit, Queen Mary Hospital
City
Hong Kong
ZIP/Postal Code
852
Country
Hong Kong

12. IPD Sharing Statement

Citations:
PubMed Identifier
21345279
Citation
Oudemans-van Straaten HM, Kellum JA, Bellomo R. Clinical review: anticoagulation for continuous renal replacement therapy--heparin or citrate? Crit Care. 2011 Jan 24;15(1):202. doi: 10.1186/cc9358.
Results Reference
background
PubMed Identifier
23424680
Citation
Leung AK, Shum HP, Chan KC, Chan SC, Lai KY, Yan WW. A retrospective review of the use of regional citrate anticoagulation in continuous venovenous hemofiltration for critically ill patients. Crit Care Res Pract. 2013;2013:349512. doi: 10.1155/2013/349512. Epub 2013 Jan 28.
Results Reference
background
PubMed Identifier
22248200
Citation
Shum HP, Chan KC, Yan WW. Regional citrate anticoagulation in predilution continuous venovenous hemofiltration using prismocitrate 10/2 solution. Ther Apher Dial. 2012 Feb;16(1):81-6. doi: 10.1111/j.1744-9987.2011.01001.x. Epub 2011 Oct 3.
Results Reference
background

Learn more about this trial

A Study on the Efficacy and Safety of Continuous Renal Replacement Therapy (CVVHDF) Using a Commercial Citrate-containing Replacement Fluid (Prismocitrate 18/0)

We'll reach out to this number within 24 hrs