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NCT05656326Active, not recruiting

Follow-up After Surgery for Colorectal Cancer

Follow-up After Surgery for Colorectal Cancer: the Prospective, Multicentre FUTURE-primary Implementation Study

Source: ClinicalTrials.gov · Last updated 25 Sept 2024

Brief summary (registry, in English)

The currently developed implementation study aims to evaluate if a patient-led home-based follow-up approach is successful, improves quality of life, reduces anxiety and lessens fear of cancer recurrence during the years after surgical treatment of colorectal cancer (CRC).

Status (registry)
Active, not recruiting
Study type
Observational
Enrollment
200 (estimated)
First submitted
2 Dec 2022
Start date
23 Aug 2021
Primary completion date
Dec 2029
Lead sponsor
Erasmus Medical Center
NCT number
NCT05656326

What you commit to

  • Study type: Observational
  • Planned participants: 200
  • From 23 Aug 2021 to the primary completion date, Dec 2029
  • 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.

Other illness

  • Patients with comorbidity or other malignancy that requires imaging of the abdomen and/or thorax every year or more frequent

Other

  • Patients with a severely complicated postoperative course, needing in hospital follow-up longer than 6 months postoperatively
  • Patients enrolled in other studies that require strict adherence to any specific follow-up practice with regular imaging - yearly or more frequent - of the abdomen and/or thorax
  • Inability to complete the questionnaires due to illiteracy and/or insufficient proficiency of the Dutch language

Who the study is looking for

  • Histologically confirmed colorectal adenocarcinoma without distant metastasis and treated with curative intent surgical resection less than 6 months ago
  • Scheduled or currently undergoing postoperative surveillance according to national guidelines
  • Written informed consent by the patient

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
Kelly Raquel Voigt
Coordinator of this site? Confirm its status
RotterdamNetherlandsUnknown status

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