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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ClinicalTrials.gov
Last refreshed on: 28 June 2021
Main ID:  NCT04937478
Date of registration: 16/06/2021
Prospective Registration: Yes
Primary sponsor: Mode Sensors AS
Public title: Correlation of Ultrafiltered Volume (UFV) to Bioimpedance Changes CTR006
Scientific title: Correlation of Ultrafiltered Volume (UFV) During Hemodialysis With a New Battery Powered, Body Worn Electronic Patch Measuring Bioimpedance.
Date of first enrolment: May 20, 2021
Target sample size: 50
Recruitment status: Recruiting
URL:  https://clinicaltrials.gov/show/NCT04937478
Study type:  Observational
Study design:   
Phase: 
Countries of recruitment
Norway
Contacts
Name:     Ellen AA Jaatun, MD PhD
Address: 
Telephone: +4747758889
Email: ellen.jaatun@modesensors.com
Affiliation: 
Key inclusion & exclusion criteria

Inclusion Criteria:

- patients scheduled for hemodialysis

- signed Informed Consent Form

Exclusion Criteria:

- acute intercurrent disease,

- subjects with known hypersensitivity to plasters (adhesive or gel).



Age minimum: 20 Years
Age maximum: N/A
Gender: All
Health Condition(s) or Problem(s) studied
Hemodialysis, Ultrafiltration, Bioimpedance
Intervention(s)
Other: Observation
Primary Outcome(s)
Correlation between ultrafiltered volume (UFV) and measured bioimpedance change [Time Frame: During hemodialysis]
Secondary Outcome(s)
Secondary ID(s)
CTR006 DELAGE 2
Source(s) of Monetary Support
Please refer to primary and secondary sponsors
Secondary Sponsor(s)
HMN Sykehuset Levanger, Norway
St. Olavs Hospital
Ethics review
Results
Results available:
Date Posted:
Date Completed:
URL:
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