NCT03482934

Brief Summary

To recognize predictors of left ventricular hypertrophy in hypertensive patients in Assiut government \& to recognize the prognostic effect of central blood pressure measurement versus office brachial blood pressure measurement.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
300

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Oct 2019

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

First Submitted

Initial submission to the registry

January 3, 2018

Completed
3 months until next milestone

First Posted

Study publicly available on registry

March 29, 2018

Completed
1.5 years until next milestone

Study Start

First participant enrolled

October 1, 2019

Completed
1 year until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 30, 2020

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

September 30, 2020

Completed
Last Updated

September 29, 2021

Status Verified

January 1, 2021

Enrollment Period

1 year

First QC Date

January 3, 2018

Last Update Submit

September 24, 2021

Conditions

HTNHypertrophy, Left Ventricular

Outcome Measures

Primary Outcomes (2)

  • Correlation between brachial blood pressure (measured by sphygmomanometer ) and left ventricular mass index measured by echocardiography to recognize predictors of left ventricular hypertrophy in HTN patients

    baseline

  • Correlation between non invasive central blood pressure (measured by mobilograph ) and left ventricular mass index (measured by echocardiography) to recognize predictors of left ventricular hypertrophy in HTN patients

    Base line

Study Arms (1)

hypertensive patients

Device: sphygmomanometerDevice: mobilograghDiagnostic Test: ECGDiagnostic Test: Echocardiography

Interventions

sphygmomanometerDEVICE

device used for measurement of brachial blood pressure

hypertensive patients
mobilograghDEVICE

device used for measurement of central blood pressure

hypertensive patients
ECGDIAGNOSTIC_TEST

Electrocardiogram

hypertensive patients
EchocardiographyDIAGNOSTIC_TEST

Echocardiography

hypertensive patients

Eligibility Criteria

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

Hypertensive patient recorded in our outpatient clinic during the last two years will be included retrospectively \& new hypertensive patients presenting to our outpatient clinic will be included prospectively for 1 year .

You may qualify if:

  • Hypertensive patient recorded in our outpatient clinic during the last two years will be included retrospectively \& new hypertensive patients presenting to our outpatient clinic will be included prospectively for 1 year .

You may not qualify if:

  • Patient aged less than 18 year old.
  • Patients from outside Assiut government .
  • Ischemic heart diasease .
  • Heart failure .
  • Cerebrovascular stroke .
  • Diabetes mellitus .
  • Patients on regular dialysis .

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Assiut university of medicine

Asyut, Egypt

Location

MeSH Terms

Conditions

Hypertrophy, Left Ventricular

Interventions

SphygmomanometersElectrocardiographyEchocardiography

Condition Hierarchy (Ancestors)

CardiomegalyHeart DiseasesCardiovascular DiseasesHypertrophyPathological Conditions, AnatomicalPathological Conditions, Signs and Symptoms

Intervention Hierarchy (Ancestors)

Diagnostic EquipmentEquipment and SuppliesHeart Function TestsDiagnostic Techniques, CardiovascularDiagnostic Techniques and ProceduresDiagnosisElectrodiagnosisCardiac Imaging TechniquesDiagnostic ImagingUltrasonography

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
CROSS SECTIONAL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal investigator

Study Record Dates

First Submitted

January 3, 2018

First Posted

March 29, 2018

Study Start

October 1, 2019

Primary Completion

September 30, 2020

Study Completion

September 30, 2020

Last Updated

September 29, 2021

Record last verified: 2021-01

Locations

EG(1)