Ignite Creation Date:
2024-05-06 @ 3:06 PM
Last Modification Date:
2024-10-26 @ 1:43 PM
Study NCT ID:
NCT04527861
Status:
RECRUITING
Last Update Posted:
2022-10-10
First Post:
2020-08-19
Brief Title:
Oncologic Outcomes of Single-incision Versus Conventional Laparoscopic Surgery for Colorectal Cancer
Sponsor:
Ruijin Hospital
Organization:
Ruijin Hospital
Study Overview
Official Title:
Oncologic Outcomes of Single-incision Laparoscopic Surgery Versus Conventional Laparoscopic Surgery for Colorectal Cancer A Multi-center Prospective Open Label Non-inferiority Randomized Controlled Trial
Status:
RECRUITING
Status Verified Date:
2022-10
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
CSILS
Brief Summary:
This study is designed to investigate long-term oncologic outcomes of single-incision laparoscopic surgery SILS compared to conventional laparoscopic surgery CLS for colorectal cancer
Detailed Description:
In order to improve cosmetic effect and reduce postoperative pain single-incision laparoscopic surgery SILS is attracting increasing attention SILS is considered to be the next major advance in the progress of minimally invasive surgical approaches to colorectal disease that is more feasible in generalized use In most previous studies SILS for colorectal cancer was feasible and short-term safe compared to conventional laparoscopic surgery CLS However there is still controversy over its potential better cosmetic effect and less postoperative pain Moreover the long-term oncologic outcomes are still inconclusive as only a few studies showed long-term survival data Up to now most studies were limited to their retrospective nature and small samples So more studies especially large-scale randomized controlled trials are needed to establish the best indications for SILS for colorectal cancer
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None