NCT01909817

Brief Summary

The investigators aim to determine whether a new method of enhancing and improving ECG acquisition, analysis and display is effective. The investigators will perform superimposition and summation of multiple standard ECG cycles, in the same lead, by temporal alignment to the peak R wave and voltage alignment to an improved baseline at the T-P segment.

Trial Health

43
At Risk

Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
300

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Jul 2013

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
unknown

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

March 20, 2013

Completed
3 months until next milestone

Study Start

First participant enrolled

July 1, 2013

Completed
28 days until next milestone

First Posted

Study publicly available on registry

July 29, 2013

Completed
3 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 1, 2013

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

August 1, 2013

Completed
Last Updated

July 29, 2013

Status Verified

July 1, 2013

Enrollment Period

1 month

First QC Date

March 20, 2013

Last Update Submit

July 24, 2013

Conditions

Outcome Measures

Primary Outcomes (1)

  • ECG Voltage spread

    We will measure the voltage spread at the S-T and P-R intervals after superimposition and summation of multiple standard ECG cycles in the same lead, by temporal alignment to the peak R wave and voltage alignment to an improved baseline at the T-P segment.

    One month

Study Arms (1)

Routine coronary angiogram patients

Procedure: Routine coronary angiogram

Interventions

Routine coronary angiogram patients

Eligibility Criteria

Age18 Years - 80 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

Patients undergoing routine coronary angiogram

You may qualify if:

  • Patients undergoing routine coronary angiogram

You may not qualify if:

  • Patients with significant irregular heart rhythm
  • Patients with heart failure

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Hillel Yaffe Medical Center

Hadera, 38100, Israel

Location

MeSH Terms

Conditions

Cardiovascular Diseases

Study Design

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

Study Record Dates

First Submitted

March 20, 2013

First Posted

July 29, 2013

Study Start

July 1, 2013

Primary Completion

August 1, 2013

Study Completion

August 1, 2013

Last Updated

July 29, 2013

Record last verified: 2013-07

Locations