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Assessment of the Interest of ANI in the Non-communicating Patient in Palliative Care (ANI-CARE)

U

University Hospital, Lille

Status

Completed

Conditions

Analgesia
Pain
End of Life

Treatments

Device: ANI

Study type

Observational

Funder types

Other

Identifiers

NCT05454202
2021_0830
2022-A00631-42 (Other Identifier)

Details and patient eligibility

About

Comfort evaluation is one of the major challenges in the palliative care setting, particularly when it comes to non-communicative patients. ANI monitoring is a non-invasive and painless technique which evaluates the parasympathetic tone activity through heart rate variability. It has proven reliable for pain assessment during general anesthesia (GA) or for sedated critically ill patients. The parasympathetic activity seems to be a good reflect of the patient's comfort, implicating stress and anxiety.

So, the ANI could be an interesting tool to assess the comfort of non-communicating end-of-life patients.

That is why the goal of our study is to assess the interest of ANI to assess the comfort of non-communicating patients hospitalized in palliative care during a painful care by comparing the ANI measure to the CPOT scale realised by the nurses in a blind manner.

Enrollment

20 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Hospitalized in palliative care Non-communicating patients (Glasgow ≤ 10)

Exclusion criteria

  • Non sinusal heart rate
  • Respiratory rate < 9/min
  • Treated by inotropes
  • Pace-maker
  • Patient in agonal phase
  • Opposition from the guardian

Trial design

20 participants in 1 patient group

Non-communicating
Description:
Non-communicating (Glasgow ≤ 10) end-of-life patient hospitalized in palliative care (age ≥ 18 years old)
Treatment:
Device: ANI

Trial contacts and locations

1

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Central trial contact

Chloe PRODHOMME, MD

Data sourced from clinicaltrials.gov

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