NCT04132947

Brief Summary

MET-REPAIR CONVAL is an international cohort study to examine the ability of self-reported exercise capacity to predict perioperative cardiovascular events correcting for preoperative risk factors.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
140

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Nov 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

October 16, 2019

Completed
5 days until next milestone

First Posted

Study publicly available on registry

October 21, 2019

Completed
11 days until next milestone

Study Start

First participant enrolled

November 1, 2019

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 28, 2020

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

February 28, 2020

Completed
Last Updated

March 2, 2020

Status Verified

February 1, 2020

Enrollment Period

4 months

First QC Date

October 16, 2019

Last Update Submit

February 28, 2020

Conditions

Anesthesia

Outcome Measures

Primary Outcomes (1)

  • Metabolic equivalents (METs)

    METs per spiroergometry; assessment at time of clinically mandated spiroergometry

    at Baseline

Study Arms (1)

Cohort

Cohort Study correlating self reported exercise activity and spiroergometry results

Eligibility Criteria

Age45 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

all patients admitted to the ambulatory cardiology ward

You may qualify if:

  • over 45 years of age
  • clinically indicated exercise testing
  • signed written informed consent

You may not qualify if:

  • unable to complete the questionnaire
  • unable to consent or unwilling to participate
  • cancelled exercise

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University Hospital Basel

Basel, 4056, Switzerland

Location

Study Officials

  • Eckhard Mauermann, Dr. med. MD

    University Hospital Basel, Dep. of Anesthesia

    PRINCIPAL INVESTIGATOR

Study Design

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

Study Record Dates

First Submitted

October 16, 2019

First Posted

October 21, 2019

Study Start

November 1, 2019

Primary Completion

February 28, 2020

Study Completion

February 28, 2020

Last Updated

March 2, 2020

Record last verified: 2020-02

Data Sharing

IPD Sharing
Will not share

Locations

CH(1)