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NCT04083482

Removal of mtDNA in Plasma by Continous Venovenous Hemofiltration in Sepsis

Status unknown NA Last updated 10 September 2019
What this trial tests

NA trial testing continous venovenous hemofiltraion in Intensive Care Unit in 20 participants. Status unknown.

Timeline
20 August 2018
Primary endpoint
20 September 2018
31 December 2019

Quick facts

Lead sponsorFirst People's Hospital of Chenzhou
PhaseNA
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment20
Start date20 August 2018
Primary completion20 September 2018
Estimated completion31 December 2019
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

First People's Hospital of Chenzhou

Who can join

18 and older, any sex, with Intensive Care Unit. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Intensive Care Unit

Currently open trials in the same condition.

Other First People's Hospital of Chenzhou trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04083482.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing