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Evaluation of a Non-invasive Urinary Collection Technique for the Adaptation of Diuretic Treatment in Incontinent Heart Failure Patient Over 75 Years of Age in the Acute Phase (ATIICA)

P

Poitiers University Hospital

Status

Enrolling

Conditions

Diuresis in Incontinent Patients

Treatments

Other: adult diaper
Other: carrying out standard care

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

Heart failure is a general disease affecting many organs and regulatory systems with a prevalence of 10% after 75 years of age, leading to significant hospitalization in the elderly. This generates a significant cost for our health system. The management of patients over 75 years of age in acute heart failure requires special monitoring of diuresis and weight. However, it is sometimes difficult to collect urine from incontinent elderly patients (not catheterized, habitually wearing protection) under intravenous diuretics. The evaluation of a non-invasive technique of urine collection for the adaptation of diuretic treatment in the incontinent patient with heart failure over 75 years of age in the acute phase seems to us to be interesting to conduct.

Enrollment

80 estimated patients

Sex

All

Ages

75 to 100 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patient over 75 years of age
  • Geriatric short-stay inpatient, geriatric/cardio medicine unit geriatrics
  • Incontinent patient with urinary protection
  • Patient with acute heart failure according to the diagnosis made by the doctors of unity
  • Patient treated with intravenous diuretic
  • Patient benefiting from a social security scheme or benefiting from it by a third party
  • Patient who gave their non-opposition to the study after clear information

Exclusion criteria

  • Patient hospitalized in another unit of the geriatric division
  • Patient allergic to the protections provided
  • Patient carrying a bladder probe upon entry into the unit
  • Patient with a precarious non-perfusable venous capital

Trial design

Primary purpose

Supportive Care

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

80 participants in 2 patient groups

The "before" period
Other group
Treatment:
Other: carrying out standard care
the "after" period
Experimental group
Treatment:
Other: adult diaper

Trial contacts and locations

1

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Central trial contact

Fanny ABRIAT; Sophie PAJOUX

Data sourced from clinicaltrials.gov

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