Late Organ Specific Adverse Effects hiPec or pElvic eXenteration

  • End date
    Sep 1, 2022
  • participants needed
  • sponsor
    University of Aarhus
Updated on 31 July 2021


The purpose of this study is to describe type and extent of organ specific late adverse effects in patients undergoing surgery for colorectal cancer with peritoneal metastases and after surgery for colorectal cancer with involvement of the urinary bladder.


After being informed about the study all patients giving written informed consent will be distributed a questionnaire asking questions on bowel function, urinary function, pain, sexual function and lymphedema. All these aspects will be investigated using validated questionnaires.

Condition Colorectal Cancer, Rectal disorder, colorectal neoplasm, colorectal cancers, cancer, colorectal, colorectal tumor, tumors, colorectal
Clinical Study IdentifierNCT04970316
SponsorUniversity of Aarhus
Last Modified on31 July 2021


Yes No Not Sure

Inclusion Criteria

Patients who have undergone intended curative CRS+HIPEC for peritoneal metastases originated from colorectal cancer (HIPEC cohort) according to national Danish guidelines
Patients who have undergone intended curative total or anterior pelvic exenteration (PE cohort) for advanced or recurrent colorectal cancer according to national Danish guidelines

Exclusion Criteria

Patients under 18 years
Patients not speaking Danish or Swedish, respectively, in Denmark and Sweden
Patients unable to give informed consent
Patients undergoing CRS+HIPEC or PE for cancers others than CRC
Terminally ill patients
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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