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The CIRE Study (CItrate REcirculation Study)

Effects of AV Port Reversal in Citrate CVVH - The CIRE Study (CItrate REcirculation Study)

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02600416
Acronym
CIRE
Enrollment
24
Registered
2015-11-09
Start date
2015-12-31
Completion date
2017-09-01
Last updated
2018-03-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Kidney Injury

Brief summary

The aim of this study is to determine the effects of AV port reversal (AVPR) on recirculation, clearance, post-filter ionized calcium and subsequently citrate dosing.

Detailed description

Rationale: AV port reversal (AVPR) has been demonstrated to increase recirculation in venous catheters used in ICU for CVVH. The effects of this frequently used manoeuvre have not been described in the setting of CVVH using regional citrate anticoagulation. Objective: The aim of this study is to determine the effects of AVPR on recirculation, clearance, post-filter ionized calcium and subsequently citrate dosing. Study design and methods: Open trial studying the effect of AVPR in patients undergoing citrate CVVH. After measurement in standard catheter configuration, AVPR is performed after which effects on catheter recirculation, clearance, citrate dosing and post-filter ionized calcium (iCa) are monitored. Sample sites: Arterial line, arterial (pre-filter) port, postfilter port (after postdilution and calcium compensation), effluent sample. All flow rates to be noted. Study population: Twelve patients admitted to intensive care, requiring continuous renal replacement therapy (CRRT) for AKI. Patients are preferably anuric and have achieved good metabolic control under CVVH before inclusion in the study.

Interventions

OTHERAV port reversal

Reversal of the AV port at 1h Reversal of the AV port to start position at 7h

Sponsors

Ziekenhuis Oost-Limburg
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Critically ill patients requiring CRRT for AKI (RIFLE criteria) * Written informed consent from the patient or legal representative * No AV port reversal had taken place before inclusion in the study * Diuresis is minimal or the patient is anuric so that effects of changes in clearance as a consequence of diuresis are minimalized and do not influence study outcomes. * The patient has undergone CVVH for a number of days, ensuring good metabolic control, so that possible short term loss of clearance as a consequence of AV port reversal has no detrimental effects.

Exclusion criteria

* pre-existing chronic renal insufficiency requiring dialysis * chronic immunosuppression * liver cirrhosis Child-Pugh C * severe or shock-related hepatitis * Pregnancy

Design outcomes

Primary

MeasureTime frame
change in citrate concentration in circuit after AV port reversal8 hours
change in post-filter ionised Ca after AV port reversal8 hours
change in clearance after AV port reversal8 hours

Countries

Belgium

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026