Impact of Dialysis Modality on Coagulation and Platelet Function

NCT ID: NCT04512131

Last Updated: 2023-12-28

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

60 participants

Study Classification

OBSERVATIONAL

Study Start Date

2020-08-04

Study Completion Date

2023-06-30

Brief Summary

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The investigators will evaluate the impact of dialysis modality (intermittent hemodialysis or continuous renal replacement therapy) in coagulation and platelet function in critically ill patients

Detailed Description

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An prospective observational study will be conducted to confirm the impact of two dialysis modalitites on coagulation and platelet function in critically ill patients requiring renal replacement therapy using laboratory test, Multiplate and ROTEM.

Conditions

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Renal Replacement Therapy

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Intermittent hemodialysis

patients who are going to undergo intermittent hemodialysis or patients who are going to switch dialysis mode to intermittent hemodialysis from continuous renal replacement therapy Laboratory test including complete blood count, prothrombin time, activated partial thromboplastin time, protein C, protein S and D-dimer, EXTEM of ROTEM and MultiplateĀ® platelet function analysis will be checked just before dialysis initiation and immediately after dialysis termination

dialysis mode

Intervention Type PROCEDURE

intermittent hemodialysis or continuous renal replacement therapy

continuous renal replacement therapy

patients who are going to undergo continuous renal replacement therapy Laboratory test including complete blood count, prothrombin time, activated partial thromboplastin time, protein C, protein S and D-dimer, EXTEM of ROTEM and Multiplate platelet function analysis will be checked within 24 hours after dialysis initiation and 48 hours after taking first blood sample

dialysis mode

Intervention Type PROCEDURE

intermittent hemodialysis or continuous renal replacement therapy

Interventions

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dialysis mode

intermittent hemodialysis or continuous renal replacement therapy

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

• Critically ill adult patients in surgical intensive care unit who require renal replacement therapy

Exclusion Criteria

* Patients treated with anti-coagulation therapy due to thrombosis/embolism
* Patients who take anti-platelet drug due to cardiac or cerebrovascular diseased
* Patients treated with pharmacological prophylaxis of deep vein thrombosis
* Patients who received blood products within 24 hours of dialysis initiation
* Patients who do not want life-sustaining care including renal replacement therapy
Minimum Eligible Age

19 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Seoul National University Hospital

OTHER

Sponsor Role lead

Responsible Party

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Ho Geol Ryu

Associate professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Seoul National University Hospital

Seoul, Jongno-gu, South Korea

Site Status

Countries

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South Korea

Provided Documents

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Document Type: Study Protocol and Statistical Analysis Plan

View Document

Other Identifiers

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Dialysis mode_coagulation

Identifier Type: -

Identifier Source: org_study_id