NCT01831297

Brief Summary

This study´s aim is to explore physiological associations concerning pulse wave velocity, heart rate and blood pressure in order to make taking the blood pressure more comfortable.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
10

participants targeted

Target at below P25 for all trials

Timeline
Completed

Started Aug 2012

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

August 1, 2012

Completed
6 months until next milestone

First Submitted

Initial submission to the registry

January 29, 2013

Completed
3 months until next milestone

First Posted

Study publicly available on registry

April 15, 2013

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 1, 2013

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

July 1, 2013

Completed
Last Updated

November 27, 2013

Status Verified

November 1, 2013

Enrollment Period

11 months

First QC Date

January 29, 2013

Last Update Submit

November 26, 2013

Conditions

Syncope

Outcome Measures

Primary Outcomes (1)

  • data about possible correlation

    Correlation between pulse wave velocity, pulse rate and blood pressure

    45 minutes

Study Arms (1)

syncope

Device: measurement of blood pressure

Interventions

measurement of blood pressureDEVICE

measurement of pulse wave velocity

syncope

Eligibility Criteria

Age18 Years - 90 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

patients with syncope

You may qualify if:

  • patients with syncope and planned tilting table investigation
  • male and female patients aged at least 18 years
  • persons being able to understand and to follow the study stuff´s instructions

You may not qualify if:

  • pregnancy or breast feeding
  • patients not being able to consent
  • cardiac pacemaker / defibrillator
  • illness of skin

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Univeristy Hospital Aachen

Aachen, North Rhine Westfalia, 52074, Germany

Location

MeSH Terms

Conditions

Syncope

Condition Hierarchy (Ancestors)

UnconsciousnessConsciousness DisordersNeurobehavioral ManifestationsNeurologic ManifestationsNervous System DiseasesSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

January 29, 2013

First Posted

April 15, 2013

Study Start

August 1, 2012

Primary Completion

July 1, 2013

Study Completion

July 1, 2013

Last Updated

November 27, 2013

Record last verified: 2013-11

Locations

DE(1)