Dissecting How Peripheral Lymphocytes Are Lost During Sepsis

NCT ID: NCT03289312

Last Updated: 2017-12-27

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

54 participants

Study Classification

OBSERVATIONAL

Study Start Date

2018-01-11

Study Completion Date

2018-12-31

Brief Summary

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There is an observational, clinical study. We recruit sepsis patients to investigate what drives peripheral lymphocyte loss in sepsis.

Detailed Description

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There is an observational, clinical study. We recruit patients with diagnosis of new onset sepsis within 24h, collect and record clinical characteristics:

①Demography data,diagnosis, admission source, infection source, APACHE II,SOFA scores;②Endotoxin levels and PaO2 measured;③Immune and systemic inflammatory indicators:T, RR, WBC, ALC, etc.;④Complicated organs dysfunctions: duration and therapy;⑤Incidence of ICU-acquired infection and prognosis.The blood samples were collected for apoptosis,necrosis,autophagy,pyroptosis measurements.The aim of this study is to investigate how peripheal lymphocyte loss relates to outcome and the mechanisms of peripheal lymphocyte loss in different condition.

Conditions

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Sepsis

Keywords

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sepsis, lymphocyte

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

PROSPECTIVE

Study Groups

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Sepsis

Diagnosis of new onset sepsis within 24h without history of tumor, hematological or immunological disease, and treatment with chemotherapy agents or corticosteroids within 6 months prior to or during the hospitalization.

No interventions assigned to this group

Health control

Health vonlunteers

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

* Health volunteers

Exclusion Criteria

* History of tumor, hematological or immunological disease, and treatment with chemotherapy agents or corticosteroids within 6 months prior to or during the hospitalization.
Minimum Eligible Age

18 Years

Maximum Eligible Age

90 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Southeast University, China

OTHER

Sponsor Role lead

Responsible Party

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Jianfeng Xie

Southeast University, China

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Zhongda Hospital

Nanjing, Jiangsu, China

Site Status

Countries

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China

Central Contacts

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Ming Xue, MD

Role: CONTACT

Phone: 08615195971003

Email: [email protected]

Other Identifiers

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2017ZDSYSLLoss

Identifier Type: -

Identifier Source: org_study_id