Early Lactate Clearance Rate in Sepsis

NCT ID: NCT04192279

Last Updated: 2019-12-10

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

UNKNOWN

Total Enrollment

220 participants

Study Classification

OBSERVATIONAL

Study Start Date

2015-01-01

Study Completion Date

2020-02-15

Brief Summary

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To assess the Influence of early lactate clearance rate monitoring in patients with sepsis.

Detailed Description

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Conditions

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Early Lactate Clearance

Keywords

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sepsis lactate early

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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lactate group

Lactate early guide resuscitation

lactate clearance

Intervention Type DIAGNOSTIC_TEST

Lactate clearance rate was monitored within 6 hours after admission

control group

early guide resuscitation without lactate

No interventions assigned to this group

Interventions

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lactate clearance

Lactate clearance rate was monitored within 6 hours after admission

Intervention Type DIAGNOSTIC_TEST

Eligibility Criteria

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Inclusion Criteria

* All patients whose blood lactate level reached or exceeded 2.0 mEq / L

Exclusion Criteria

* Incomplete clinical data
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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The Second Hospital of Hebei Medical University

OTHER

Sponsor Role lead

Responsible Party

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Fei Tong

Director

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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The Second Hospital of Hebei Medical University

Shijiazhuang, Hebei, China

Site Status RECRUITING

Countries

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China

Central Contacts

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Fei Tong, Dr.

Role: CONTACT

Phone: +8615803210603

Email: [email protected]

Jiangqing Xu, Dr.

Role: CONTACT

Phone: +8615732193221

Email: [email protected]

Facility Contacts

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Fei Tong, Dr.

Role: primary

Other Identifiers

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78247891400

Identifier Type: -

Identifier Source: org_study_id