Predictive Value of Dynamic Combination of BNP and NGAL for the Prognosis of Patients With Sepsis

NCT ID: NCT02871544

Last Updated: 2016-08-18

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

124 participants

Study Classification

INTERVENTIONAL

Study Start Date

2015-06-30

Study Completion Date

2016-02-29

Brief Summary

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Objective: to clarify the predictive value of brain natriuretic peptide (BNP) in combination with neutrophil gelatinase associated lipocalin (NGAL) for the prognosis of patients with sepsis.

Detailed Description

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Conditions

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28-day Mortality Sepsis

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

FACTORIAL

Primary Study Purpose

SCREENING

Blinding Strategy

NONE

Study Groups

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Low BNP and Low NGAL Group

BNP≤100pg/ml and NGAL≤153pg/ml

Group Type SHAM_COMPARATOR

BNP and NGAL

Intervention Type OTHER

High BNP and Low NGAL Group

BNP\>100pg/ml and NGAL≤153pg/ml

Group Type ACTIVE_COMPARATOR

BNP and NGAL

Intervention Type OTHER

Low BNP and High NGAL Group

BNP≤100pg/ml and NGAL\>153pg/ml

Group Type ACTIVE_COMPARATOR

BNP and NGAL

Intervention Type OTHER

High BNP and High NGAL Group

BNP\>100pg/ml and NGAL\>153pg/ml

Group Type ACTIVE_COMPARATOR

BNP and NGAL

Intervention Type OTHER

Interventions

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BNP and NGAL

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* age ≥18 years and \<85 years;
* presence of severe sepsis according to Survival Sepsis Campaign 10;
* all patients voluntarily joined this study with informed consents.

Exclusion Criteria

* participated in other trials within 30 days before the criteria for this trial were met;
* expected to die within 24 hours;
* pregnant;
* advanced malignancy with life expectancy \<6 months;
* history of congestive heart failure;
* chronic renal dysfunction (baseline creatinine \>176.8μmol/L); and
* relatives were unwilling to agree to the use of full life support.
Minimum Eligible Age

18 Years

Maximum Eligible Age

80 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Southeast University, China

OTHER

Sponsor Role lead

Responsible Party

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Chun Pan

Dr

Responsibility Role PRINCIPAL_INVESTIGATOR

Other Identifiers

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Zhongda Hospital AKI

Identifier Type: -

Identifier Source: org_study_id

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