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Comparative Effectiveness of Oxiris Hemofilters Versus Conventional Hemofilters in Septic Patients

NCT ID: NCT06735365

Last Updated: 2024-12-31

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

426 participants

Study Classification

OBSERVATIONAL

Study Start Date

2024-05-23

Study Completion Date

2024-12-01

Brief Summary

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We divided patients in 2 groups. First group was the patients who received Oxiris filters during CRRT. Second group was the patiens who have received CRRT filters other than Oxiris.

We compared the lab parameters (Urea, Creatinin, Lactate, ABG parameters and SOFA escore with together.

Detailed Description

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Conditions

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Sepsis - to Reduce Mortality in the Intensive Care Unit Hemodiafiltration Cytokine

Study Design

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Observational Model Type

COHORT

Study Time Perspective

RETROSPECTIVE

Study Groups

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Oxiris

The group which we used oxiris filter for CRRT.

CRRT

Intervention Type OTHER

Hemodiafiltration

Non-Oxiris

The group which we used other filters like M150 for CRRT.

CRRT

Intervention Type OTHER

Hemodiafiltration

Interventions

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CRRT

Hemodiafiltration

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

sepsis diagnosis CRRT indication

Exclusion Criteria

patients under age of 18
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Bakirkoy Dr. Sadi Konuk Research and Training Hospital

OTHER_GOV

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Bakirkoy Dr Sadi Konuk Research and Training Hospital

Istanbul, , Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Other Identifiers

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2024-05-02

Identifier Type: -

Identifier Source: org_study_id