ClinicalTrials.Veeva

Menu

Wearable Health Technology for Perioperative Risk Assessment (WELCOME)

I

Istituto Clinico Humanitas

Status

Completed

Conditions

Surgery--Complications

Treatments

Other: 6 Minute walking test
Other: Frailty questionaires

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

Accurate and timely preoperative identification of high-risk patients provides opportunities to better inform and manage them. Current predictors for perioperative complications are either resource consuming or have low accuracy. The primary objective of the study is to assess if Wearable Devices may be an alternative to assess cardiopulmonary function, with low risks and lower costs.

Enrollment

31 patients

Sex

All

Ages

70+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age 70 or more
  • Undergoing major non cardiac surgery
  • Expected surgical duration > 2 hours.

Exclusion criteria

  • Patients unable to express consent
  • Patients undergoing urgent/emergent surgery
  • Patients in which surgery is planned within less than two weeks
  • Patients with limited physical activity due to limited mobility related with neurological or orthopedic disease
  • Acute cardiovascular event
  • Surgery conducted in locoregional anesthesia only

Trial design

31 participants in 1 patient group

Adult patients undergoing major surgery
Description:
Patients aged 70 or older undergoing major non cardiac surgery, with expected surgical duration \> 2 hours.
Treatment:
Other: Frailty questionaires
Other: 6 Minute walking test

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems