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NCT04412980 Clinical Trial

Ionized Magnesium for Monitoring of Citrate-anticoagulated CVVHD

Intensive Care Unit Syndrome Clinical Trial

— MagiCC  

Official title:
Importance of Ionized Magnesium Measurement for Monitoring of Continuous Venovenous Haemodialysis With Citrate Anticoagulation

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT04412980
Other study ID # RECHMPL20_0121
Secondary ID
Status Completed
Phase
First received
Last updated
Start date May 1, 2020
Est. completion date November 23, 2020

Study information
Verified date May 2020
Source University Hospital, Montpellier
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

It has been reported in several studies that ionized hypomagnesemia is associated with higher morbidity and mortality rates. During continuous renal replacement therapy with regional citrate anticoagulation (CRRT-RCA), the loss of magnesium has been reported to not be covered by magnesium concentration in ordinary dialysis fluid. This may lead to ionized hypomagnesemia. However the incidence of ionized hypomagnesemia in patients requiring CRRT-RCA remains unclear and need to be estimated to determine if ionized magnesium monitoring could be of interest. This study aim to assess the incidence of ionized hypomagnesemia induced by CRRT-RCA.

Recruitment information / eligibility
Status Completed
Enrollment 40
Est. completion date November 23, 2020
Est. primary completion date October 1, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years to 100 Years
Eligibility Inclusion criteria: - Consecutive patients admitted to the ICU and requiring continuous renal replacement therapy with regional citrate anticoagulation - age > 18 ans Exclusion criteria: - Persons under protection - Paritcipation rejections

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
France Uhmontpellier Montpellier

Sponsors (2)
Lead Sponsor Collaborator
University Hospital, Montpellier Novamedica Laboratories

Country where clinical trial is conducted

France, 

Outcome
Type Measure Description Time frame Safety issue
Primary assess the systemic ionized magnesemia change after 24h of CRRTsystemic variations of iMg assess the systemic ionized magnesemia change after 24h of CRRT wiith regional citrate anticoagulation Day 0 and Day 1
Secondary Proportion of patients with heart rhythm disturbances Proportion of patients with heart rhythm disturbances 1 day
Secondary Assessment of morbidity and mortality Assessment of morbidity and mortality 1 day
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