Pain in Oncolgy: Evaluation of a Non Invasive Monitoring Device (ANI). A Monocentric Prospective Study (ANIONCO)

Hopital Foch

Status: Completed

Conditions: Cancer; Pain

Treatments: Device: Non Invasive Monitoring Device (ANI)

Study type: Interventional

Funder types: Other

Identifiers

NCT02902627

2011-A01559-32 (Other Identifier)

2011/64

Details and patient eligibility

About

l'ANI (Analgesia Nociception Index

The main objective of the research is to estimate the Analgesia Nociception Index (ANI) as a parameter giving the possibility of measuring the pain in painful metastatic cancer. The parameter ANI is compared with visual analogical scale (VAS) score.

Enrollment: 80 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• more than 18 years, -no legal protection, -
• life expectancy is considered over 3-months
• not receiving of béta-blocking,
• Having a rhythm sinusal without extrasystole
• benefiting from a coverage by a social security system

Exclusion criteria

• Pace-Maker
• Diabetes mellitus

Trial design

Primary purpose: Other

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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80 participants in 1 patient group

Metastatic cancer

Experimental group

Treatment:

Device: Non Invasive Monitoring Device (ANI)