Early Renal Replacement Therapy and the Outcome of Acute Kidney Injury

NCT ID: NCT01819038

Last Updated: 2016-01-28

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

Clinical Phase

NA

Total Enrollment

60 participants

Study Classification

INTERVENTIONAL

Study Start Date

2013-01-31

Study Completion Date

2015-12-31

Brief Summary

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This research project is a prospective study to compare mortality between early renal replacement therapy (RRT) and late renal replacement therapy by using plasma neutrophil gelatinase associated lipocalin (pNGAL) as a tool in decision- making.

Detailed Description

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Conditions

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Acute Renal Failure

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Participants Investigators

Study Groups

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High NGAL and early RRT

NGAL level \> 400 ng/ml and start continuous renal replacement therapy early

Group Type EXPERIMENTAL

continuous renal replacement therapy

Intervention Type PROCEDURE

High NGAL and late RRT

NGAL \> 400 ng/ml and start continuous renal replacement therapy late

Group Type EXPERIMENTAL

continuous renal replacement therapy

Intervention Type PROCEDURE

Low NGAL

NGAL \< 400 ng/ml and starting continuous renal replacement therapy follow with absolute indication

Group Type ACTIVE_COMPARATOR

continuous renal replacement therapy

Intervention Type PROCEDURE

Interventions

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continuous renal replacement therapy

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* The patient must have given his/her informed and signed consent
* patients with acute kidney injury in the intensive care ward.

Exclusion Criteria

* The patient refuses to sign the consent
* The patient is pregnant, parturient, or breastfeeding
* End stage renal disease
* Chronic renal failure
* previous kidney transplant
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Chulalongkorn University

OTHER

Sponsor Role lead

Responsible Party

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Nattachai Srisawat ,M.D.

Principle Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Nattachai Srisawat, M.D.

Role: PRINCIPAL_INVESTIGATOR

Chulalongkorn University

Locations

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King Chulalongkorn Memorial Hospital

Bangkok, Bangkok, Thailand

Site Status

Countries

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Thailand

References

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Fayad AI, Buamscha DG, Ciapponi A. Timing of kidney replacement therapy initiation for acute kidney injury. Cochrane Database Syst Rev. 2022 Nov 23;11(11):CD010612. doi: 10.1002/14651858.CD010612.pub3.

Reference Type DERIVED
PMID: 36416787 (View on PubMed)

Other Identifiers

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chula

Identifier Type: -

Identifier Source: org_study_id

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