Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID06850688

Impact of Ambulatory Continuous Monitoring Using Remote Monitoring Medicine Within Patient's Care Pathway Following Colorectal Surgery - A Multicenter Randomized Study

Led by Nantes University Hospital · Updated on 2026-03-19

362

Participants Needed

14

Research Sites

N/A

Total Duration

On this page

Sponsors

N

Nantes University Hospital

Lead Sponsor

E

EPOCA U&I

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are evaluating the impact of using a remote monitoring platform to support patients after colorectal surgery who are at risk of being readmitted to the hospital. The study compares the effectiveness of 30 days of remote monitoring after discharge versus the conventional discharge process. The goal is to see if the remote monitoring can reduce hospital readmission and improve recovery in patients who have undergone colorectal surgery. Participants are randomly assigned to one of two groups: one group receives usual care with a conventional discharge and follow-up visits, while the other group uses the remote monitoring platform for 30 days after leaving the hospital. The remote platform connects patients and healthcare professionals through devices like oximeters, blood pressure monitors, and other tools to track health status. Both groups have a routine postoperative visit at 30 days and a follow-up phone call at 90 days. Patients also keep a diary of healthcare use during the 90 days. During the study, participants will attend standard postoperative assessments and complete questionnaires on quality of life and satisfaction. Researchers will monitor hospital readmissions, complications, recovery milestones such as return of bowel function, and overall healthcare use over 90 days. The study includes interviews and focus groups with patients and healthcare providers to gather qualitative feedback. Safety and medical-economic outcomes will also be evaluated throughout the 90-day follow-up period.

CONDITIONS

Brief Title

Impact of Ambulatory Continuous Monitoring Using Remote Monitoring Medicine Within Patient's Care Pathway Following Colorectal Surgery (CONTACT-GRECCAR 21)

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Man or woman over 18 years old at the time of the J0 visit
  • Patient who underwent colorectal surgery less than 28 days ago or is scheduled to undergo colorectal surgery not managed as an outpatient procedure
  • Underwent resection of at least one colonic or rectal segment and/or an anastomosis involving the colon or rectum
  • Meets at least one of these: anticipated early discharge (within 24 hours after laparoscopic surgery without stoma, or within 5 days after laparotomy and/or surgery with stoma and/or rectal surgery), or estimated risk of hospital readmission greater than 10% according to the specified score
  • Patient affiliated with a health insurance plan
  • Patient who has signed the study consent form
Not Eligible

You will not qualify if you...

  • Discharge to a rehabilitation center requested by the patient
  • Condition managed on an outpatient basis in routine practice
  • Patient eligible for home hospitalization services
  • Suicidal or hetero-aggressive risk in a patient living alone at home
  • Homeless patient
  • Pregnant or breastfeeding women
  • Patient under legal guardianship, curatorship, or protected legal status
  • Patient already enrolled in an interventional postoperative follow-up study

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Surgery

Duration - Day 0

Participants undergo colorectal surgery as part of their treatment.

1 visit (in-person)

Post-operative Follow-up

Duration - 30 days after hospital discharge

Participants are monitored after hospital discharge either through standard care or a remote monitoring platform for 30 days to track recovery and health status.

1 routine postoperative consultation visit on Day 30 and phone contact on Day 90

Long-term Monitoring

Duration - 90 days after hospital discharge

Participants complete a patient diary from Day 0 to Day 90 to record healthcare utilization and are contacted by phone at Day 90 for final follow-up.

1 phone contact on Day 90

Trial Site Locations

Total: 14 locations

1

CHU Angers

Angers, France

Actively Recruiting

2

Clinique Tivoli- Ducos

Bordeaux, France

Actively Recruiting

3

CHU Grenoble

Grenoble, France

Actively Recruiting

4

Centre Hospitalier Lyon-Sud

Lyon, France

Actively Recruiting

5

CHU Timone - Assistance publique-Hôpitaux de Marseille

Marseille, France

Actively Recruiting

6

Hôpital Nord - Assistance publique- Hôpitaux de Marseille

Marseille, France

Actively Recruiting

7

Institut Paoli Calmettes

Marseille, France

Not Yet Recruiting

8

CHU Nantes

Nantes, France

Actively Recruiting

9

Hôpital de Bicêtre - Assistance Publique Hôpitaux de Paris

Paris, France

Actively Recruiting

10

Hôpital Saint Antoine - Assistance publique - Hôpitaux de Paris

Paris, France

Actively Recruiting

11

CHU Rennes

Rennes, France

Actively Recruiting

12

Clinique Mutualiste de l'estuaire

Saint-Nazaire, France

Actively Recruiting

13

CHU Toulouse

Toulouse, France

Actively Recruiting

14

CHRU Tours

Tours, France

Actively Recruiting

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Research Team

E

Emilie DUCHALAIS

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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