ClinConnect ClinConnect Logo
Search / Trial NCT06914245

Personalized Care Pathways for Bowel Symptoms in Rectal Cancer Patients_contributing Factors (Treatable)

Launched by KU LEUVEN · Mar 31, 2025

Trial Information

Current as of July 09, 2025

Not yet recruiting

Keywords

Bowel Diary Quality Of Life (Qo L) Care Pathway

ClinConnect Summary

This clinical trial is focused on understanding bowel symptoms that some patients experience after treatment for rectal cancer. Rectal cancer can be treated with surgery, which often leads to issues like diarrhea or difficulty controlling bowel movements, affecting the patient’s quality of life. This study aims to identify the factors that contribute to these ongoing bowel problems a year after surgery, with the goal of creating better care plans to help manage these symptoms and improve overall well-being.

To participate in this trial, individuals must be at least 18 years old, able to read and speak Dutch, and scheduled for specific types of rectal surgery, like Total Mesorectal Excision (TME) or Partial Mesorectal Excision (PME). Participants will need to give their written consent before joining. It’s important to note that people who have had other types of surgeries or conditions affecting bowel function may not be eligible. By participating, patients can help researchers learn more about their symptoms and how to better support others in similar situations.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Voluntary written informed consent of the participant or their legally authorized representative has been obtained prior to any screening procedures.
  • At least 18 years of age at the time of signing the Informed Consent Form (ICF).
  • Proficient in reading, comprehending, and conversing in Dutch.
  • Patients scheduled for Total Mesorectal Excision (TME) or Partial Mesorectal Excision (PME) or 'Watch and wait' protocol due to rectal cancer.
  • Exclusion Criteria:
  • The participant has undergone a different type of surgery, including a Hartmann procedure, abdominoperineal excision, transanal endoscopic microsurgery, or sigmoid resection.
  • Experienced fecal incontinence prior to undergoing surgery.
  • Are affected by neurological disorders affecting bowel function.
  • Already underwent previous pelvic surgery, previous pelvic radiation or rectal surgery for non-cancer reasons.
  • Has a permanent stoma.

About Ku Leuven

KU Leuven, a prestigious research university located in Belgium, is renowned for its commitment to advancing medical science and improving patient care through innovative clinical trials. With a strong emphasis on interdisciplinary collaboration, KU Leuven integrates cutting-edge research with clinical practice, facilitating the development of new therapeutic strategies and medical technologies. The institution's robust infrastructure and expertise in various fields, including biotechnology, pharmacology, and public health, position it as a leader in conducting high-quality clinical research that adheres to rigorous ethical standards and regulatory requirements. Through its clinical trials, KU Leuven aims to contribute significantly to the global biomedical landscape and enhance health outcomes for diverse populations.

Locations

Leuven, Vlaams Brabant, Belgium

Patients applied

0 patients applied

Trial Officials

Inge Geraerts, PhD

Principal Investigator

KU Leuven

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported