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OpenTrials
Completed

NCT Number: NCT04937478

Correlation of Ultrafiltered Volume (UFV) to Bioimpedance Changes

Patient submitted to hemodialysis are followed through a dialysis - interim - dialysis cycle.

No intervention is done. Additional blood tests and clinical tests are used as pseudo-endpoints. Correlation is made to ultrafiltrated volume (UFV).

Completed

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Key information

Age range

20 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Levanger Hospital, Levanger, Norway

Loading trial locations.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • patients scheduled for hemodialysis
  • signed Informed Consent Form

Exclusion criteria

  • acute intercurrent disease,
  • subjects with known hypersensitivity to plasters (adhesive or gel).

Treatment and study plan

observation

Other

Only observational study, no intervention.

Primary outcomes

  1. Correlation between ultrafiltered volume (UFV) and measured bioimpedance change

    Time frame: During hemodialysis

    A change in measured thoracic bioimpedance is expected to correlate to UFV

Sponsors and collaborators

Lead sponsor

Mode Sensors AS

Industry

Collaborators

  • Helse Nord-Trøndelag HF
  • St. Olavs Hospital

Registry information

Official study title

Correlation of Ultrafiltered Volume (UFV) During Hemodialysis With a New Battery Powered, Body Worn Electronic Patch Measuring Bioimpedance.

Acronym: CTR006

Important dates

Study start
2021
Primary completion
2021
Study completion
2021
First posted
Jun 24, 2021
Registry last updated
Apr 18, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.