Correlation of Ultrafiltered Volume (UFV) to Bioimpedance Changes (CTR006)

M

Mode Sensors

Status

Completed

Conditions

Hemodialysis, Ultrafiltration, Bioimpedance

Treatments

Other: Observation

Study type

Observational

Funder types

Other
Industry

Identifiers

NCT04937478
CTR006 DELAGE 2

Details and patient eligibility

About

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).

Enrollment

31 patients

Sex

All

Ages

20+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • patients scheduled for hemodialysis
  • signed Informed Consent Form

Exclusion criteria

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

Trial design

31 participants in 1 patient group

Hemodialysis patients
Description:
Patients who undergo hemodialysis in hospital every two to three days.
Treatment:
Other: Observation

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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