Ignite Creation Date:
2024-10-25 @ 7:52 PM
Last Modification Date:
2024-10-26 @ 3:38 PM
Study NCT ID:
NCT06567756
Status:
NOT_YET_RECRUITING
Last Update Posted:
None
First Post:
2024-01-02
Brief Title:
Conformal Sphincter-Preservation Operation Versus InterSphincteric Resection on Anal Function in Low Rectal Cancer
Sponsor:
None
Organization:
None
Study Overview
Official Title:
A Multicenter Prospective Randomized Controlled Clinical Trial of the Effect of Conformal Sphincter-preservation Operation Versus Intersphincteric Resection on Postoperative Anal Function in Patients With Low Rectal Cancer
Status:
NOT_YET_RECRUITING
Status Verified Date:
2024-01
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
No
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
In this clinical trial the investigators compared anal function genitourinary function quality of life perioperative safety and oncological prognosis after CSPO for patients with low rectal cancer using ISR as a control to provide high-level evidence-based medical evidence for the choice of anorectal preservation surgical approaches for patients with low rectal cancer
Detailed Description:
The CSPO surgical approach is a series of targeted improvements designed primarily on the basis of analyzing the causes of poor postoperative function of the ISR while building on research on the ultrastructure of the pelvic floor anal canal For these reasons the investigators designed the present study to compare anal function quality of life perioperative safety and oncologic prognosis after CSPO for patients with low rectal cancer using ISR surgery as a control and to provide high-level evidence-based medical evidence for the choice of anorectal preservation surgical modalities for patients with low rectal cancer
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None