Recruiting

CCPC

Sponsor:

Medtronic - MITG

Code:

NCT06638073

Conditions

Surgical Procedure, Unspecified

Intensive Care Units (ICUs)

Eligibility Criteria

Sex: All

Age: 19+

Healthy Volunteers: Not accepted

Study Details

Brief summary:

To confirm feasibility and accessibility of the CCPC Platform (Oxymotion, Bridge Health Solutions medication adherence software, CloudDX home kit) in two different environments - in hospital and at-home, in patients undergoing non-cardiac surgery.

Conditions

Surgical Procedure, Unspecified

Intensive Care Units (ICUs)

Study ID

NCT06638073

Start date

Mar 13, 2025

Status verified date

May, 2025

Completion date

Jun 20, 2026

Anticipated

Primary completion date

Jun 20, 2026

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 19+

Healthy Volunteers: Not accepted

Inclusion Criteria:

  • 19 years or older
  • Patients that have undergone a non-cardiac surgery at SPH requiring an inpatient hospital stay
  • Peri-op patients who are in the Surgical High Acuity Unit (SHAU) and those followed by Anesthesia Perioperative Outreach team on the ward
  • Living within British Columbia, Canada and in an area that is covered by Bell cellular network

Exclusion Criteria:

  • Patient refusal
  • Lack of capacity to consent to the study (including having received sedative or general anesthetic within the past 24 hours)
  • Unable to use (or does not have a caregiver who can help put on) study monitoring device at home
  • Unable to complete (or does not have a caregiver who can help complete) study questionnaires by electronic (mobile, tablet, or computer), paper, nor phone
  • No access to cell phone nor landline at home to receive follow-ups
  • Preoperatively known to be discharged to a nursing home or rehabilitation facility
  • Known allergic reactions to any part material of study devices

Study Design

Enrollment

50 participants

Anticipated

Interventions and Outcome Measures

Primary outcome measure

  • Collect patient and clinicians' feedback about the CCPC Platform [ Time Frame: From enrollment to the end of follow up at 10 days ]
  • Confirm the technical goals of the CCPC platform are met. [ Time Frame: From enrollment to the end of follow up at 10 days ]
  • Collect patient and clinicians' feedback about the CCPC Platform [ Time Frame: From enrollment to the end of follow up at 10 days ]
  • Collect patient and clinicians' feedback about the CCPC Platform [ Time Frame: From enrollment to the end of follow up at 10 days ]
  • Confirm the technical goals of the CCPC platform are met. [ Time Frame: From enrollment to the end of follow up at 10 days ]
  • Confirm the technical goals of the CCPC platform are met. [ Time Frame: From enrollment to the end of follow up at 10 days ]

Central Contacts and Locations

Central contacts

Elise Huisman

+1 236-308-4876elise.huisman@medtronic.com

Locations

Saint Pauls Hospital

Recruiting

Vancouver, British Columbia, Canada, V6Z 1Y6

Contacts

Ronald Ree, MD

rree@providencehealth.bc.ca

More Information

Sponsor

Medtronic - MITG

Last update posted

Mar 12, 2026

Last verified

May, 2025

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by Medtronic - MITG on 2026-03-12.