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Search / Trial NCT06850688

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

Launched by NANTES UNIVERSITY HOSPITAL · Feb 24, 2025

Trial Information

Current as of June 27, 2025

Recruiting

Keywords

Colorectal Surgery Remote Monitoring Platform Hospital Length Of Stay Rehospitalization

ClinConnect Summary

The CONTACT-GRECCAR 21 trial is looking at how effective remote monitoring can be after colorectal surgery. This means that after patients leave the hospital, they will either be monitored from home for 30 days or follow the usual discharge process without extra monitoring. The goal is to see if remote monitoring helps reduce the chances of patients needing to return to the hospital.

To be eligible for this trial, participants must be at least 18 years old and have had colorectal surgery that required a hospital stay. They should also be at risk for readmission, meaning there’s a good chance they might need to go back to the hospital after surgery. If you participate, you'll have a follow-up visit at the hospital 30 days after your surgery and a phone call 90 days later to check on your recovery. This study is not currently recruiting participants, so if you or a loved one are interested, it's important to stay updated on when enrollment begins.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria :
  • Man or woman over 18 years old at the time of the J0 visit,
  • Patient who has undergone colorectal surgery not managed on an outpatient basis at the investigator center,
  • * At least one of the following two criteria:
  • Anticipated early discharge (within 24 hours following laparoscopic surgery without diversion and within 5 days following surgery by laparotomy with stoma) for a surgery not managed on an outpatient basis 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.

About Nantes University Hospital

Nantes University Hospital, a leading academic medical institution in France, is dedicated to advancing healthcare through innovative research and clinical trials. As a prominent sponsor of clinical studies, the hospital integrates cutting-edge scientific exploration with patient care, fostering collaborations among multidisciplinary teams of healthcare professionals and researchers. With a strong emphasis on ethical standards and patient safety, Nantes University Hospital aims to contribute to the development of effective therapies and interventions that enhance patient outcomes and overall public health.

Locations

Nantes, , France

Angers, , France

Rennes, , France

Tours, , France

Grenoble, , France

Marseille, , France

Toulouse, , France

Lyon, , France

Saint Nazaire, , France

Bordeaux, , France

Marseille, , France

Marseille, , France

Paris, , France

Paris, , France

Patients applied

0 patients applied

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported