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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06409403
Other study ID # YB2017
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date January 1, 2017
Est. completion date December 31, 2025

Study information

Verified date May 2024
Source The Third Xiangya Hospital of Central South University
Contact Bo Yi, MD
Phone 13786179533
Email yibo2018pro@126.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Intraoperative pelvic autonomic nerve (PAN) injury is the dominant reason for genitourinary malfunction after total mesorectal excision (TME), particularly in low rectal tumours. TME necessitates meticulous, sharp dissection with an awareness of the PAN pathway. In particular, laparoscopic TME (L-TME) is technically difficult and requires advanced laparoscopic surgical skills. Comparing with the conventional laparoscopic approach, 3D vision, surgeon-manipulated camera systems, and multi-degree-of-freedom robotic instruments facilitate identification and preservation of the PAN during robotic-assisted TME (R-TME), theoretically facilitating favourable recovery of postoperative genitourinary function. Previous studies have mostly focused on the impact of advanced robotic technologies on postoperative functions. However, in addition to robotic surgical technology, postoperative function is impacted by multiple other intricate factors, such as oncology, comorbidities, postoperative complications, and adjuvant chemoradiotherapy. Consequently, the superiority of robotic surgery in terms of recovery of postoperative genitourinary function has been controversial in previous studies. Hence, to comprehensively evaluate the effect of robotic technology on postoperative genitourinary function, we conducted a prospective controlled study comparing the conventional approach and robotic surgery.


Recruitment information / eligibility

Status Recruiting
Enrollment 164
Est. completion date December 31, 2025
Est. primary completion date December 31, 2025
Accepts healthy volunteers No
Gender All
Age group 18 Years to 85 Years
Eligibility Inclusion Criteria: (i) lesions that were determined by histopathological examination and were staged preoperatively using pelvic MRI and CT scans; (ii) patients aged =18 and = 75 years; and (iii) American Society of Anesthesiology (ASA) class =3 Exclusion Criteria: Benign prostate hyperplasia, previous bladder or prostate surgery, severe sexual dysfunction (International Index of Erectile Function (IIEF) score <10 or Female Sexual Function Index (FSFI) score =26.55), urgent operation, simultaneous or heterochronous multiple primary rectal tumours, distant metastasis, or other severe cardiopulmonary complications.

Study Design


Related Conditions & MeSH terms


Intervention

Device:
clinical application of robotic technique
effect of various surgical technique on clinical efficacy of TME

Locations

Country Name City State
China The Third Xiangya Hospital of Central South University Changsha Hunan

Sponsors (1)

Lead Sponsor Collaborator
general surgery 3

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary International Prostate Symptom Score (IPSS) evaluation of genitourinary function preoperation,1?3?6?12 months after operation
Secondary International Index of Erectile Function (IIEF) evaluation of genitourinary function preoperation,1?3?6?12 months after operation
Secondary Female Sexual Function Index (FSFI) evaluation of genitourinary function preoperation,1?3?6?12 months after operation
Secondary operative time operative outcomes perioperative
Secondary blood loose operative outcomes perioperative
Secondary conversion operative outcomes perioperative
Secondary retrieved lymph nodes operative outcomes perioperative
Secondary complete TME specimens operative outcomes perioperative
Secondary circumferential resection margins (CRMs) operative outcomes perioperative
Secondary complication operative outcomes perioperative
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