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Status unknownNCT04083482Updated Sep 10, 2019

Removal of mtDNA in Plasma by Continous Venovenous Hemofiltration in Sepsis

An interventional study of continous venovenous hemofiltraion in Intensive Care Unit, sponsored by First People's Hospital of Chenzhou. Status unknown at 1 site in China. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2019-09-10.

Sponsored by First People's Hospital of Chenzhou · Not applicable, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Sep 2019), so the status shown — last known as Enrolling by invitation — may be out of date.

From the registry’s dates

  • Registered 1 year after the study started (first participant enrolled Aug 2018, registered Sep 2019).
Phase
Not applicable
Study type
Interventional
Enrollment
20
Allocation
Not applicable
Ages
18 Years and older
Sex
All
01

Study summary

The plasma level of mtDNA in sepsis is affected by continous venovenous hemofiltation(CVVH)

Read the detailed description

Continous renal replacement therapy (CRRT)has become routine for patients with chronic renal failure ,AKI,fliud overload as well as oliguria in ICU .In clinical patients ,continous venovenous hemofoiltration (CVVH)is actually the method of chioce for CRRT in critically ill and hemodynamic instable patients .CVVH has significant beneficial effects on removing inflammatory cytokines ,improving oxygen index,increasing cardiac index and regulating immune dysfuntion .

02

Conditions studied

  • Intensive Care Unit

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Keywords

  • Mitochondrial DNA
  • Sepsis
  • Continous venovenous hemofiltation
  • Intensive Care Unit
03

In context

Sepsis

1,899 studies on the registry are indexed under Sepsis; 462 are open to participants now.

This study's enrollment of 20 is below the median of 105 across 896 interventional studies indexed under Sepsis.

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Lead sponsor

First People's Hospital of Chenzhou is the lead sponsor of 11 studies on the registry; 3 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

Adult septic patients undergoing CRRT

Exclusion criteria

Exclusion Criteria:

  1. Missing vists
  2. transplatation
  3. cancer
  4. aquired immunodeficiency syndrome
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
20 participants (actual)

Study arms

  • Experimental
    Septic patients require CVVH

    continuous 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 .

    Procedure: continous venovenous hemofiltraion

Interventions

  • Procedurecontinous venovenous hemofiltraion

    CVVH

06

What researchers measure

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.

    Time frame: befor,6hours, 12hours, after CVVH treatment

07

Study locations

1 site
  • The First Hospital of Chenzhou
    Chenzhou, Hunan 450003, China
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 10, 2019, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT04083482
Lead sponsor
First People's Hospital of Chenzhou
Responsible party
Xingui Dai (Critical Care Medicine, First People's Hospital of Chenzhou) — Principal investigator
First posted
Sep 10, 2019
Start date
Aug 20, 2018
Primary completion
Sep 20, 2018
Completion
Dec 31, 2019 (estimated)
Last update
Sep 10, 2019

Study contacts

dixian luo, MS
study director · Chenzhou First people Hospital

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Sep 2019. You cannot join it, but the record below documents what was studied.

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