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Evaluation of Continuous Non Invasive Blood Pressure With Adult Volunteers

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General Electric (GE)

Status

Unknown

Conditions

Blood Pressure

Treatments

Device: measuring blood pressure with noninvasive blood pressure device

Study type

Interventional

Funder types

Industry

Identifiers

NCT04876664
210080046

Details and patient eligibility

About

A study to collect data recorded by devices for cNIBP evaluation purposes.

Full description

The study is going to be conducted to collect data from the devices used in the study for future AMS engineering purposes as deemed appropriate by the Sponsor.

Enrollment

12 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Healthy male or female, aged 18 years or older (≥18 years);
  • Willing and able to give informed consent for participation in the study;
  • Able and willing to comply with all the study requirements.

Exclusion criteria

  • Who is pregnant or lactating;
  • Who is a smoker;
  • Who has consumed alcohol in the last 24 hours;
  • Who has been previously diagnosed with Ataxia or balance disorder;
  • Who has been previously diagnosed with Raynaud's disease/ syndrome/ phenomenon;
  • Who has been previously a diagnosed cardiovascular condition requiring medication or has an internal pacemaker;
  • Who has an injury, deformity, A-V fistula, or other characteristic limiting the placing of cuffs on arms/fingers;

Trial design

Primary purpose

Diagnostic

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

12 participants in 1 patient group

Ambulatory monitoring solution
Experimental group
Description:
this study has only one arm
Treatment:
Device: measuring blood pressure with noninvasive blood pressure device

Trial contacts and locations

0

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Central trial contact

Juha Pärkkä

Data sourced from clinicaltrials.gov

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