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Clinical Trials/NCT02902627
NCT02902627
Completed
Not Applicable

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

Hopital Foch1 site in 1 country80 target enrollmentAugust 2012
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ConditionsPainCancer

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Pain
Sponsor
Hopital Foch
Enrollment
80
Locations
1
Primary Endpoint
Comparison of the ANI parameter with the VAS
Status
Completed
Last Updated
8 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSitesSimilar Trials

Overview

Brief Summary

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.

Registry
clinicaltrials.gov
Start Date
August 2012
End Date
August 2016
Last Updated
8 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

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

Outcomes

Primary Outcomes

Comparison of the ANI parameter with the VAS

Time Frame: 4 hours

Study Sites (1)

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