Evaluation of Continuous Non Invasive Blood Pressure With Adult Volunteers

NCT ID: NCT04876664

Last Updated: 2021-05-06

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

12 participants

Study Classification

INTERVENTIONAL

Study Start Date

2021-06-01

Study Completion Date

2021-09-01

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

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

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

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.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Blood Pressure

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

DIAGNOSTIC

Blinding Strategy

NONE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Ambulatory monitoring solution

this study has only one arm

Group Type EXPERIMENTAL

measuring blood pressure with noninvasive blood pressure device

Intervention Type DEVICE

To measure blood pressure in different circumstances with noninvasive blood pressure device

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

measuring blood pressure with noninvasive blood pressure device

To measure blood pressure in different circumstances with noninvasive blood pressure device

Intervention Type DEVICE

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

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;
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

GE Healthcare

INDUSTRY

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Juha Pärkkä

Role: PRINCIPAL_INVESTIGATOR

VTT

Central Contacts

Reach out to these primary contacts for questions about participation or study logistics.

Juha Pärkkä

Role: CONTACT

+35840-7530525

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

210080046

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.