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NCT07113717Not yet recruiting

Post Operative Hospital at Home After Colorectal Surgery

Early Post-operative Discharge of Colorectal Surgical Patients to a Virtual Hospital at Home Model (Post Operative Hospital at Home) - a Clinical Feasibility Study

Source: ClinicalTrials.gov · Last updated 11 Aug 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

The goal of this feasibility study is to investigate whether a virtual Hospital at Home is safe and possible for patients undergoing planned minimally invasive colorectal surgery. The study aims to answer the following main questions: What are the patient- and next-of-kin-related effects, as well as the clinical and organizational effects, of home-based admission? What are the implementation barriers for a full-scale randomized controlled trial? Participants will follow a standardized protocol for their care befor, during and after surgery. However, the care after surgery will be conducted at home using telemedicine.

Status (registry)
Not yet recruiting
Study type
Interventional
Enrollment
20 (estimated)
First submitted
7 Jul 2025
Start date
15 Dec 2025
Primary completion date
31 Dec 2026
Lead sponsor
Nordsjaellands Hospital
NCT number
NCT07113717

What you commit to

  • Study type: Interventional
  • Planned participants: 20
  • From 15 Dec 2025 to the primary completion date, 31 Dec 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Complications during surgery warranting in-hospital admission (observation in intensive care unit or close observation from other specialities, e.g. cardiology)

Other illness

  • Conversion to emergency surgery (uncontrolled perforation of bowel, ileus)

Other

  • Patients who cannot comply with self-assessment
  • Improficiency in Danish
  • Pregnancy

Who the study is looking for

  • Planned minimally invasive (laparoscopic or robot-assisted) CRS
  • No epidural analgesia
  • No new stoma
  • Bleeding \< 500 ml
  • Actual condition assessed to be clinically stable
  • Meeting the Chung score discharge criteria for ambulatory surgery
  • Self-reliant or receives sufficient formal care to be care-independent of a primary informal caregiver
  • Home-based admission will be located within catchment area of the hospital (according to the official address of the individual)
  • Signed informed written and oral consent

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Department of Surgery
Coordinator of this site? Confirm its status
HillerødDenmarkUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.