About this trial
The aim of this cohort study is to record, evaluate and compare the surgical, oncological as well as the functional outcome and Quality of life after mesorectal excision for rectal cancer
Eligibility criteria
Qualifiers
Men and Women >18 years
Patients with rectal cancer
Underwent mesorectal excision
Agreed to fill in a validated questionnaires before surgery and after stoma reversal
Disqualifiers
Age < 18
No informed consent (no general consent, no consent to use personal data for research purpose)
Trial design
Treatments tested in this trial
- Total mesorectal excision for rectal cancer
Treatment groups
250 Participants
are divided into 1 treatment groupSponsors and collaborators
Source ClinicalTrials.gov