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NCT02964429

Determination In-vivo KUF for Diacap Pro Hemodialyser

Completed NA Last updated 7 February 2017
What this trial tests

NA trial testing Diacap Pro High-Flux in Kidney Failure,Chronic in 12 participants. Completed in 23 December 2016.

Timeline
14 November 2016
Primary endpoint
23 December 2016
23 December 2016

Quick facts

Lead sponsorB.Braun Avitum AG
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposebasic science
Enrollment12
Start date14 November 2016
Primary completion23 December 2016
Estimated completion23 December 2016
Sites1 location across Czechia

Drugs / interventions tested

Conditions studied

Sponsor

B.Braun Avitum AG

Who can join

18 and older, any sex, with Kidney Failure,Chronic or Renal Insufficiency,Chronic. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The main purpose of this study is the determination of the in-vivo ultrafiltration coefficient (in-vivo KUF) for Diacap Pro dialyzers following routine dialysis prescription in the United States.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other recruiting trials for Kidney Failure,Chronic

Currently open trials in the same condition.

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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/NCT02964429.

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