Optimization of Ureterolysis During Hysterectomy

Status Withdrawn

Clinical Trial Summary

The purpose of this study is to improve the safety of surgery to remove a uterus (a hysterectomy) by better understanding where a patient's ureters lie.

Clinical Trial Description

Objectives:

Primary: (While uterus is under tension)

- To determine the shortest distance from the ureter to the uterine vessels.

- To determine the distances from the ureter to the gonadal vessels in infundibulo-pelvic (IP) at the pelvic sidewall. This will be defined at the distance from the IP ligament at the level of the pelvic sidewall to the point on the ureter directly below these vessels

- To determine the distances from the ureter to the gonadal vessels in the infundibulo-pelvic (IP) ligament at the point where the gonadal vessels enter in to the ovary. This will be defined as the distance from where the vessels in the IP enter the ovary to the point on the ureter directly below this.

Secondary

- To determine thermal spread from the Ligasure, and Harmonic device using H&E and Movat staining.

- To determine the burst pressure of segments of IP ligament that have undergone Ligasure or Harmonic electrosurgery. ;

Study Design

Related Conditions & MeSH terms

Hysterectomy

Clinical Trial Details

NCT number	NCT03123315
Study type	Interventional
Source	Case Comprehensive Cancer Center
Contact
Status	Withdrawn
Phase	N/A
Start date	April 2018
Completion date	June 2020

View Details

See also
Status	Clinical Trial	Phase
Recruiting	`NCT05337566` - Does Additional Use of Preoperative Azithromycin Decrease Posthysterectomy Infections	N/A
Recruiting	`NCT04130464` - Intraperitoneal Infusion of Analgesic for Postoperative Pain Management	Phase 4
Recruiting	`NCT05537727` - Robotic MIS With Dexter
Completed	`NCT05037383` - Motion and Viewing Analysis of Surgeons During Minimally Invasive Gynecological Interventions	N/A
Completed	`NCT04080323` - Single-dose Vaginal Dinoprostone and Hysterectomy	Phase 3
Not yet recruiting	`NCT06011538` - Web-based Versus Standard Information for Same Day Hysterectomy (WISH)	N/A
Completed	`NCT03187327` - Feasibility of Opportunistic Salpingectomy at the Time of Vaginal Hysterectomy for Benign Pathology	N/A
Completed	`NCT00528177` - Morphine vs. Oxycodone for Postoperative Pain Management	Phase 4
Terminated	`NCT00551785` - Surveillance Study of Women Taking Intrinsa®	Phase 4
Completed	`NCT03641625` - Effect of SmtO2 Guided Care on PONV (iMODIPONV)	N/A
Terminated	`NCT03500744` - Erector Spinae Plane Block for Major Gynecologic and Urologic Surgery	N/A
Recruiting	`NCT03294343` - Risk-Reducing Surgeries for Hereditary Ovarian Cancer	N/A
Completed	`NCT03610425` - A Standardized Bundle Protocol to Optimize Outcomes With Patients Undergoing Gynecological Surgery
Completed	`NCT05659303` - Evaluation of an Outpatient Protocol in Patients Operated for Laparoscopic Hysterectomy
Completed	`NCT05270447` - Short-Term Effects of Connective Tissue Massage After Hysterectomy	N/A
Recruiting	`NCT05031182` - Tolerance of the vNOTES Surgical Technique in Total Hysterectomy for Benign Lesion. Clinical Trial of Non-inferiority Compared to the Laparoscopic Technique.	N/A
Completed	`NCT03634306` - Ultravision Visual Clearing System in Laparoscopic Hysterectomy and Myomectomy	N/A
Completed	`NCT01526668` - Follow-up Strategies for Improved Postoperative Recovery After Benign Hysterectomy	N/A
Recruiting	`NCT05374720` - Analysis of the Molecular Composition of Tubal Cilia in Patients With or Without Ectopic Pregnancy	N/A
Recruiting	`NCT04109989` - Clinical Assessment - HominisTM Surgical System	N/A