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CompletedNCT04132947MET-REPAIR ValUpdated Mar 2, 2020

Validity of the MET-REPAIR Questionnaire

An observational study in Anesthesia, sponsored by University Hospital, Basel, Switzerland. Completed at 1 site in Switzerland. Open to participants aged 45 Years and older. Per ClinicalTrials.gov, last updated 2020-03-02.

Sponsored by University Hospital, Basel, Switzerland · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
140
Ages
45 Years and older
Sex
All
01

Study 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.

02

Conditions studied

  • Anesthesia
03

In context

Lead sponsor

University Hospital, Basel, Switzerland is the lead sponsor of 968 studies on the registry; 191 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
45 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

all patients admitted to the ambulatory cardiology ward

Inclusion criteria

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

Exclusion criteria

Exclusion Criteria:

  • unable to complete the questionnaire
  • unable to consent or unwilling to participate
  • cancelled exercise
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
140 participants (actual)
Patient registry
No

Groups and cohorts

  • Cohort

    Cohort Study correlating self reported exercise activity and spiroergometry results

06

What researchers measure

Primary outcomes

  1. Metabolic equivalents (METs)

    METs per spiroergometry; assessment at time of clinically mandated spiroergometry

    Time frame: at Baseline

07

Study locations

1 site
  • University Hospital Basel
    Basel, 4056, Switzerland
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 2, 2020, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT04132947
Lead sponsor
University Hospital, Basel, Switzerland
Responsible party
Sponsor
First posted
Oct 21, 2019
Start date
Nov 1, 2019
Primary completion
Feb 28, 2020
Completion
Feb 28, 2020
Last update
Mar 2, 2020

Study contacts

Eckhard Mauermann, Dr. med. MD
principal investigator · University Hospital Basel, Dep. of Anesthesia

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Feb 2020. You cannot join it, but the record below documents what was studied.

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Discussion

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