C48.0
Conditions
Interventions
Group 1: Patients with primary retroperitoneal sarcomas who underwent surgery (with colorectal resection) at DKG-certified sarcoma centres or hospitals that fulfil certification-equivalent criteria du
Sponsors
Universitätsklinikum Mannheim, Medizinische Fakultät Mannheim der Universität Heidelberg
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: - Histological confirmation with verification of a retroperitoneal sarcoma - Previous tumor resection with colorectal resection - Surgery in a DKG-certified sarcoma center or hospital that fulfills certification-equivalent criteria - Age from 18 years - Written consent
Exclusion criteria
Exclusion criteria: - Missing consent
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Evaluation of resection and reconstruction procedures of the colon and rectum in the context of multivisceral resections of retroperitoneal sarcomas. | — |
Secondary
| Measure | Time frame |
|---|---|
| -Evaluation of postoperative complications associated with resections and reconstructions of the colon during and after multivisceral resections of retroperitoneal sarcomas (Comprehensive Complication Index (CCI), up to 90 days postoperatively). -Assessment of health-related quality of life after colorectal resections in the context of RPS resections (using standardized questionnaires) -Assessment of changes in bowel function after resection of retroperitoneal sarcomas -Identification of problems and needs of RPS patients who have undergone resection and reconstruction of the colon, e.g. with regard to education, home care, bowel function, stoma care, rehabilitation measures and therapy intensity and sequence. Determination of the influence of the following patient-, tumor- and treatment-related factors on the above-mentioned primary and secondary study objectives: - Gender - age - Body Mass Index (BMI) - Malnutrition (serum albumin preoperatively) - Concomitant diseases (e.g. diabetes mellitus, coronary heart disease) - Previous abdominal surgery - Size, localization (left/right), grading and histological subtype of the RPS - Neoadjuvant therapies (radiotherapy and/or chemotherapy) - Operation time - Intraoperative blood loss - Extent of the surgical procedure | — |
Countries
Germany, Switzerland
Contacts
Public ContactJens Jakob
Chirurgische Klinik, Universitätsmedizin Mannheim
Outcome results
None listed