intented enterostoma in patients with colorectal carcinoma
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: -patients with positive proof of colorectal cancer or highly suspected for colorectal cancer.-Curative intentions - - Minimum Age 18.- sufficient knowledge of german language to understand patients consent and questionnaires.- physical and psychological ability to take part in this study.- written patients consent
Exclusion criteria
Exclusion criteria: under 18 years.- palliative Intention in the thearapy.- akute psychological diseases.- missing written consent.- participation in study testing different operative techniques
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Is there a difference between anticipated Quality of life and actually experienced Quality of life in Patients suffering from colorectal cancer expecting an enterostoma ? This is a systematic structered study with a specially for this Topic designed questionnaire. The Patients answer the questionnaires at difened intervalls. The first one will be handed out in the outpatients clinic (Special colorectal cancer clinic).The second will be answered the day before the Operation (ward) after the opprtunity of a consultation with a specially trained stoma-nurse (Consultation facultative, second questionnaire mandatory). The postoperative questionnaires are done at 3 and 6 month after the Operation (during outpatient clinic). The fifth questionnaire is for those patients facing the anastomosis and loss of stoma operation (on the ward). Primary question ist wether there is a difference between anticipated quality of life and expierienced quality of life in colorecatal caner patients facing an enterostoma. A further aim of this study (prinary aim) ist to define parameter wich might lead to an improvement of quality of life in colorecalt cancer patients expecting to get an enterostoma / having an enterostoma. If there can be Parameter defined to improve the Quality of life further studies should follow. | — |
Secondary
| Measure | Time frame |
|---|---|
| Does the preoperative conversation with the Stoma nurse change the anticipated qualitiy of life? Is there a difference in the subgroupanalysis? Can parameter for pre- or postopeative Intervention be identified to improve the Quality of life for intervention ? Can there be a total score generated from individual parts of the questionnaire? | — |
Countries
Germany
Contacts
Univesitätsklinik für Allgemein- und ViszeralchirurgieKlinikum Oldenburg AöR