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Comparison of RCA and RACD in Extra-renal Purification by SLED (ARDC-SLED)

Primary Purpose

Acute Kidney Injury

Status
Recruiting
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Sustained Low-Efficiency Dialysis
Sponsored by
Groupe Hospitalier Sud Ile-de-France
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Acute Kidney Injury

Eligibility Criteria

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

Inclusion Criteria:

  • All patient requiring Renal replacement Therapy

Exclusion Criteria:

  • Age < 18 years
  • Pregnancy
  • Hypercalcemia ≥ 3 mmol/L.
  • Major under guardianship
  • Major deprived of liberty
  • Impossible to obtain free and informed consent
  • Presence of hemostasis or coagulation disorders:
  • Thrombocytopenia < 30 G/L.
  • Curative anticoagulation.
  • Severe liver disease with PT<30%.
  • Coagulation factor deficit.
  • Non-membership in a social security system.

Sites / Locations

  • Groupe Hospitalier Sud Ile-de-FranceRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Other

Other

Arm Label

Group 1: RACD - RCA

Group 2 : RCA - RACD

Arm Description

First period of treatment with Regional Anticoagulation by Citrate-Free Decalcification SLED and second period of treatment with Regional Citrate Anticoagulation SLED

First period of treatment with Regional Citrate Anticoagulation SLED and second period of treatment with Regional Anticoagulation by Citrate-Free Decalcification SLED

Outcomes

Primary Outcome Measures

Measurement of the plasma urea
We will compare plasma urea clearance after reaching the prescribed session time without irreversible coagulation of the extracorporeal circuit, with both methods tested in the study.

Secondary Outcome Measures

Measurement of the concentration of Ca²+i in post-filter
Measurement at different timepoints after the beginning of the concentration of Ca²+i in post-filter during each RRT session.
Measurement of the concentration of Ca²+i (patient)
Measurement at different timepoints after the beginning of the concentration of Ca²+i (patient) during each RRT session.
Measurement of the concentration of Mg2+
Measurement of the concentration of Mg2+ at the end of each RRT session.
Measurement of heart rate during each RRT session.
Measurement heart rate during each RRT session.
Measurement of blood pressure
Measurement of blood pressure during each RRT session.
Number of circuit losses during each RRT session,
Number of circuit losses during each RRT sessions,
Number of catheter thrombosis during each RRT session
Number of catheter thrombosis during each RRT session

Full Information

First Posted
June 8, 2021
Last Updated
January 12, 2023
Sponsor
Groupe Hospitalier Sud Ile-de-France
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1. Study Identification

Unique Protocol Identification Number
NCT04968587
Brief Title
Comparison of RCA and RACD in Extra-renal Purification by SLED
Acronym
ARDC-SLED
Official Title
Comparison of Regional Citrate Anticoagulation (RCA) and Regional Anticoagulation by Citrate-Free Decalcification in Renal (RACD) Replacement Therapy Using Sustained Low-Efficiency Dialysis
Study Type
Interventional

2. Study Status

Record Verification Date
January 2023
Overall Recruitment Status
Recruiting
Study Start Date
February 1, 2022 (Actual)
Primary Completion Date
September 16, 2023 (Anticipated)
Study Completion Date
September 16, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Groupe Hospitalier Sud Ile-de-France

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
One of the main RRT issues is anticoagulation of the ECC, because blood contact with biomaterials causes bio-incompatibility reactions, including activation of the coagulation cascade. Based on Regional Citrate Anticoagulation (RCA) protocols, an ionized calcium (Ca-ion) concentration around 0.25 to 0.35mmol / L prevents fibrino formation and allows anticoagulation for the ECC. During RCA, metabolic side effects may occur due to systemic flow of citrate. Our postulate is that reduction of ionized calcemia related to the use of a calcium-free dialysate and haemofilter performance makes it possible to avoid citrate infusion. Our study aim to compare intermittent RRT using 4% Citrate infusion and without Citrate.
Detailed Description
Background: Renal Replacement Therapy (RRT), requires anticoagulation of the extracorporal circuit (ECC) using heparin, citrate or repeated rinsing. Difficulties of implementation or exposition to complications (thrombosis, hemorrhage or electrolyte disorder) are frequent. Purpose: Regional anticoagulation of the ECC based on ionized calcemia reduction, as using citrate, but induced by the use of a calcium-free dialysate associated with the performance of the hemofilter could reduce these risks and the cost of intermittent RRT. This study aims to compare the efficiency of a regional anticoagulation technique based on the reduction of Ionized Calcium in the extracorporal circuit, without the use of Citrate and with Citrate during intermittent RRT. Abstract: One of the main RRT issue is anticoagulation of the ECC, because blood contact with biomaterials causes bio-incompatibility reactions, including activation of the coagulation cascade. Based on Regional Citrate anticoagulation (RCA) protocols, an ionized calcium (Ca-ion) concentration around 0.25 to 0.35mmol/L prevents fibrino formation and allows anticoagulation for the ECC. During RCA, metabolic side effects may occur due to systemic passage of citrate. Our postulate is that reduction of ionized calcemia related to the use of a calcium-free dialysate and haemofilter performance makes it possible to avoid citrate infusion. Our study aims at comparing intermittent RRT using 4% Citrate infusion and without Citrate.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Kidney Injury

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
138 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Group 1: RACD - RCA
Arm Type
Other
Arm Description
First period of treatment with Regional Anticoagulation by Citrate-Free Decalcification SLED and second period of treatment with Regional Citrate Anticoagulation SLED
Arm Title
Group 2 : RCA - RACD
Arm Type
Other
Arm Description
First period of treatment with Regional Citrate Anticoagulation SLED and second period of treatment with Regional Anticoagulation by Citrate-Free Decalcification SLED
Intervention Type
Procedure
Intervention Name(s)
Sustained Low-Efficiency Dialysis
Other Intervention Name(s)
intermittent haemodialysis equipment with lower blood flow and dialysate flow combined with prolonged sessions
Intervention Description
All patient requiring Renal replacement Therapy in the intensive care unit will be randomized in open order (cross-over) with either Regional anticoagulation with Citrate or Regional anticoagulation by Decalcification without Citrate
Primary Outcome Measure Information:
Title
Measurement of the plasma urea
Description
We will compare plasma urea clearance after reaching the prescribed session time without irreversible coagulation of the extracorporeal circuit, with both methods tested in the study.
Time Frame
up to 8 hours
Secondary Outcome Measure Information:
Title
Measurement of the concentration of Ca²+i in post-filter
Description
Measurement at different timepoints after the beginning of the concentration of Ca²+i in post-filter during each RRT session.
Time Frame
30 minutes, 1 hour; 4 hours and 8 hours
Title
Measurement of the concentration of Ca²+i (patient)
Description
Measurement at different timepoints after the beginning of the concentration of Ca²+i (patient) during each RRT session.
Time Frame
30minutes, 1 hour; 4 hours and 8 hours
Title
Measurement of the concentration of Mg2+
Description
Measurement of the concentration of Mg2+ at the end of each RRT session.
Time Frame
8 hours
Title
Measurement of heart rate during each RRT session.
Description
Measurement heart rate during each RRT session.
Time Frame
Hour 0; 30 minutes; 60 minutes; 90 minutes; 120 minutes; 150 minutes; 180 minutes; 210 minutes; 240 minutes; 270 minutes; 300 minutes; 330 minutes; 360 minutes; 390 minutes; 420 minutes; 450 minutes; 480 minutes
Title
Measurement of blood pressure
Description
Measurement of blood pressure during each RRT session.
Time Frame
Hour 0; 30 minutes; 60 minutes; 90 minutes; 120 minutes; 150 minutes; 180 minutes; 210 minutes; 240 minutes; 270 minutes; 300 minutes; 330 minutes; 360 minutes; 390 minutes; 420 minutes; 450 minutes; 480 minutes
Title
Number of circuit losses during each RRT session,
Description
Number of circuit losses during each RRT sessions,
Time Frame
Hour 0; 480 minutes
Title
Number of catheter thrombosis during each RRT session
Description
Number of catheter thrombosis during each RRT session
Time Frame
Hour 0; 480 minutes

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: All patient requiring Renal replacement Therapy Exclusion Criteria: Age < 18 years Pregnancy Hypercalcemia ≥ 3 mmol/L. Major under guardianship Major deprived of freedom Impossible to obtain free and informed consent Presence of hemostasis or coagulation disorders: Thrombocytopenia < 30 G/L. Curative anticoagulation. Severe liver disease with Prothrombin rate <30%. Coagulation factor deficit. Not registered to a social security system.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Herve DJOMGANG
Phone
+33181742721
Email
drc.promotion@ghsif.com
First Name & Middle Initial & Last Name or Official Title & Degree
Arezki AGHER
Phone
+33181742228
Email
arezki.agher@ghsif.fr
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Franck Pourcine, MD
Organizational Affiliation
Groupe Hospitalier Sud Ile-de-France
Official's Role
Principal Investigator
Facility Information:
Facility Name
Groupe Hospitalier Sud Ile-de-France
City
Melun
ZIP/Postal Code
77000
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Franck Pourcine, MD
Phone
+33181742085
Email
franck.pourcine@ghsif.fr
First Name & Middle Initial & Last Name & Degree
Franck Pourcine, MD

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Comparison of RCA and RACD in Extra-renal Purification by SLED

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