Perioperative and Postoperative Evaluation of Rectal and Urogenital Function in Patients Undergoing Rectal Resection

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorTechnische Universität Dresden

About this trial

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.

Eligibility criteria

Qualifiers

Patients undergoing rectal resection with total mesorectal excision

Disqualifiers

primary or secondary removal of rectal sphincter apparatus

patients with enterostomy persisting 12 months after initial rectal resection

Trial design

Treatments tested in this trial

  • Rectal resection

Treatment groups

No treatment groups listed