Evaluating rectal and urogenital function after rectal surgery
Perioperative and Postoperative Evaluation of Rectal and Urogenital Function in Patients Undergoing Rectal Resection
Technische Universität Dresden · NCT05257746
This study looks at how rectal surgery affects bowel and bladder function in patients to see what might cause problems afterwards and improve recovery.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 500 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Technische Universität Dresden (other) |
| Locations | 1 site (Dresden, Saxony) |
| Trial ID | NCT05257746 on ClinicalTrials.gov |
What this trial studies
This study systematically analyzes the perioperative and postoperative development of rectal and urogenital function in patients undergoing rectal resection with total mesorectal excision. It aims to identify risk factors associated with loss of urogenital and sphincter function following the procedure. By understanding these risk factors, the study seeks to inform tailored postoperative treatment strategies that could enhance patient outcomes. The findings could significantly impact clinical management for patients with rectal cancer.
Who should consider this trial
Good fit: Ideal candidates are patients scheduled for rectal resection with total mesorectal excision.
Not a fit: Patients who have had primary or secondary removal of the rectal sphincter apparatus or those with a persistent enterostomy for over 12 months may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved functional outcomes and tailored postoperative care for patients undergoing rectal surgery.
How similar studies have performed: While this study focuses on a specific patient cohort, similar studies have shown that understanding functional outcomes post-surgery can lead to improved management strategies.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patients undergoing rectal resection with total mesorectal excision Exclusion Criteria: * primary or secondary removal of rectal sphincter apparatus * patients with enterostomy persisting 12 months after initial rectal resection
Where this trial is running
Dresden, Saxony
- Department of Gastrointestinal-, Thoracic and Vascular Surgery University Hospital Carl Gustav Carus Technische Universität Dresden — Dresden, Saxony, Germany (RECRUITING)
Study contacts
- Principal investigator: Johannes Fritzmann, Dr. — Technische Universität Dresden
- Study coordinator: Johannes Fritzmann, Dr.
- Email: johannes.fritzmann@ukdd.de
- Phone: +49 351 458 19477
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Rectal Surgery