K57 K63 C18
Conditions
Interventions
Group 1: Questionnaire before surgery (T0), 1 week after (T1), 3 months after (T2), 6 months after (T3), 12 months after (T4)
Sponsors
Klinik für Allgemein-, Viszeral- und Transplantationschirurgie LMU, Klinikum der Universität München Campus Großhadern
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: all patients undergoing colorectal resections without the need for a stoma and age > 18 years
Exclusion criteria
Exclusion criteria: inflammatory bowel disease, need for a stoma, multivisceral resections, additional abdominal malignancies influencing bowel function (e.g. peritoneal tumour spread), missing of informed consent, lacking capability to answer the questionnaires
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Rate of LARS after oncologic and non-oncologic colorectal resections, depending on the type of resection • Anterior rectal resections • Sigmoid resections • Left sided resection • Proximal colonic resections (any resection proximal to the left sided transverse colon) | — |
Secondary
| Measure | Time frame |
|---|---|
| Development of LARS-symptoms over time, Need for stool-medication after surgery for symptom-control, Impact of emergency-procedures on occurrence of LARS, Impact of oncologic and non-oncologic resections on occurrence of LARS, Effect of symptoms on patients’ daily life | — |
Countries
Germany
Contacts
Public ContactSandra Sehmisch
Klinik für Allgemein-, Viszeral- und Transplantationschirurgie Klinikum der Universität München Koordinationszentrum Chirurgische Studien
Outcome results
None listed