NCT06360224

Brief Summary

This is a post-market observational, non-interventional, multicenter clinical investigation with the purpose of harvesting high quality data from regular cardiac bypass surgery (CABG).

Trial Health

65
Monitor

Trial Health Score

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

Enrollment
100

participants targeted

Target at P50-P75 for all trials

Timeline
37mo left

Started May 2024

Longer than P75 for all trials

Status
not yet recruiting

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 Progress40%
May 2024May 2029

First Submitted

Initial submission to the registry

April 6, 2024

Completed
5 days until next milestone

First Posted

Study publicly available on registry

April 11, 2024

Completed
1 month until next milestone

Study Start

First participant enrolled

May 15, 2024

Completed
5 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 15, 2029

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

May 15, 2029

Last Updated

April 11, 2024

Status Verified

April 1, 2024

Enrollment Period

5 years

First QC Date

April 6, 2024

Last Update Submit

April 6, 2024

Conditions

Outcome Measures

Primary Outcomes (1)

  • Wide and high-quality dataset uploaded to CaseCloud from CABG-procedures.

    1 day

Interventions

The objective of this study is to harvest a wide dataset of high quality to allow exploratory analysis and training of machine learning

Eligibility Criteria

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

Patients scheduled for cardiac bypass surgery (CABG) that have signed an informed consent form for this study

You may qualify if:

  • Patient older than 18 years
  • Scheduled for CABG
  • Understand the nature of the procedure and willingness to comply with the CIP
  • Provide written informed consent

You may not qualify if:

  • Patient younger than 18 years
  • Any condition that the investigator believes should exclude participation

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Central Study Contacts

Study Design

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

Study Record Dates

First Submitted

April 6, 2024

First Posted

April 11, 2024

Study Start

May 15, 2024

Primary Completion (Estimated)

May 15, 2029

Study Completion (Estimated)

May 15, 2029

Last Updated

April 11, 2024

Record last verified: 2024-04