Removal of mtDNA in Plasma by Continous Venovenous Hemofiltration in Sepsis
1 other identifier
interventional
20
1 country
1
Brief Summary
The plasma level of mtDNA in sepsis is affected by continous venovenous hemofiltation(CVVH)
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Aug 2018
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
August 20, 2018
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 20, 2018
CompletedFirst Submitted
Initial submission to the registry
September 3, 2019
CompletedFirst Posted
Study publicly available on registry
September 10, 2019
CompletedStudy Completion
Last participant's last visit for all outcomes
December 31, 2019
CompletedSeptember 10, 2019
September 1, 2019
1 month
September 3, 2019
September 5, 2019
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Change of mtDNA concentration in plasma
The specimens in the prefilter and postfilter blood as well as in the ultrafiltrate were obtained at the beginning of CRRT (T0) and 6 h (T6h), 12 h (T12h) after the setup of CVVH.
befor,6hours, 12hours, after CVVH treatment
Study Arms (1)
Septic patients require CVVH
EXPERIMENTALcontinuous venovenous hemofiltration. Continuous renal replacement therapy(CRRT)has become routine for patients with chronic renal failure ,AKI,fliud overload as well as oliguria in ICU .Continuous venovenous hemofiltration(CVVH)is the method of chioce for CRRT in critical ill .CVVH has significant beneficial effects on removing inflammatory cytokines ,improving oxygen index ,decreasing vasopressor requirements,increasing cardiac index and regulating immune dysfunction .
Interventions
Eligibility Criteria
You may qualify if:
- Adult septic patients undergoing CRRT
You may not qualify if:
- Missing vists
- transplatation
- cancer
- aquired immunodeficiency syndrome
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
The First Hospital of Chenzhou
Chenzhou, Hunan, 450003, China
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY DIRECTOR
dixian luo, MS
Chenzhou First people Hospital
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Critical Care Medicine
Study Record Dates
First Submitted
September 3, 2019
First Posted
September 10, 2019
Study Start
August 20, 2018
Primary Completion
September 20, 2018
Study Completion
December 31, 2019
Last Updated
September 10, 2019
Record last verified: 2019-09