Actively Recruiting
Perioperative and Postoperative Evaluation of Rectal and Urogenital Function in Patients Undergoing Rectal Resection
Led by Technische Universität Dresden · Updated on 2024-06-13
500
Participants Needed
1
Research Sites
486 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The aim of this study is the systematic analysis of the development of perioperative rectal and urogenital function in patients undergoing rectal resection with total mesorectal excision and the identification of risk factors for urogenital and sphincter function loss after this procedure. Knowledge of the corresponding risk factors could enable the identification of patient cohorts that could benefit from an intensified or altered postoperative treatment path. The results of this study could thus significantly influence the clinical management of patients with rectal cancer and improve the functional outcome in the long term.
CONDITIONS
Official Title
Perioperative and Postoperative Evaluation of Rectal and Urogenital Function in Patients Undergoing Rectal Resection
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients undergoing rectal resection with total mesorectal excision
You will not qualify if you...
- Primary or secondary removal of rectal sphincter apparatus
- Patients with enterostomy persisting 12 months after initial rectal resection
AI-Screening
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Trial Site Locations
Total: 1 location
1
Department of Gastrointestinal-, Thoracic and Vascular Surgery University Hospital Carl Gustav Carus Technische Universität Dresden
Dresden, Saxony, Germany, 01307
Actively Recruiting
Research Team
J
Johannes Fritzmann, Dr.
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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