Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06850688

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

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

362

Participants Needed

14

Research Sites

99 weeks

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

The goal of this Clinical Investigation is to evaluate the effectiveness of implementing the discharge protocol of the remote monitoring platform after colorectal surgery in patients at risk of hospital readmission. Participants will be randomized into either the "30 days of remote monitoring" group or the "conventional discharge" group. The patient returns to the site for their postoperative visit at 30 days and is contacted by phone 90 days after their surgery.

CONDITIONS

Official 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...

Inclusion Criteria :

  • Man or woman over 18 years old at the time of the J0 visit,
  • Patient who underwent surgery less than 28 days ago, or who is scheduled to undergo colorectal surgery not managed as an outpatient procedure at the investigational center, including resection of at least one colonic or rectal segment and/or an anastomosis involving the colon or rectum,
  • At least one of the following two criteria:
  • Anticipated early discharge (within 24 hours following laparoscopic surgery without stoma and without diversion, and within 5 days following laparotomy and/or surgery with stoma and/or rectal surgery) for a procedure that is not usually managed as an outpatient surgery in routine practice,
  • Estimated risk of hospital readmission greater than 10% according to the nomogram of Tevis et al. [15], adapted to the postoperative context in digestive surgery (>120 points according to this score).
  • Patient affiliated with a health insurance plan,
  • Patient who has signed the study consent form.

Exclusion Criteria:

  • Discharge to a rehabilitation center requested by the patient,
  • Condition managed on an outpatient basis in routine practice for this type of patient,
  • 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.
Not Eligible

You will not qualify if you...

History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety

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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

CONTACT

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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