The Effect of Partial Bladder Filling on Post-operative Time to Void in

Status Completed

Clinical Trial Summary

The purpose of this study is to determine if partially filling the bladder after laparoscopic/robotic gynecologic surgery (for benign disease) shortens the time required to spontaneously void for patients to determine if this subsequently shortens patient stay times in the Post Anesthesia Care Unit (PACU) following surgery. This intervention would be compared to the current standard of care, which involves removing the patient's Foley catheter with an empty bladder and then giving the patient up to 6 hours to void in the PACU.

Clinical Trial Description

Patients undergoing laparoscopic/robotic hysterectomy or myomectomy who meet the study criteria will be contacted by the research assistant at a pre-operative visit. The risks and benefits of participation will be explained to them. If they choose to participate they will sign the consent form at that time. At the time of the surgery, the research coordinator will open a sealed envelope containing the patient's assignment to partial bladder filling or no bladder filling. The research coordinator will then notify the surgeon via secure phone call or secure messaging service and the patient/subject will have their bladder partially filled or completely emptied as relayed to the surgeon at the end of the procedure in the Operating Room, unless there are issues of patient safety or operative complications. In the patients who are chosen for partial bladder filling, the bladder will be back-filled with 150 cc of normal saline and then the Foley catheter will be removed at the end of the procedure. In patients who have no bladder filling, the bladder will be completely emptied and then the Foley catheter will be removed. One of the providers who perform the gynecological surgical procedures will be responsible for back-filling or completely emptying the bladder with the Foley catheter. The patients will be followed in the PACU to determine the time it takes for them to void. The will also be followed for any complications until they are four weeks post surgery. The electronic medical record will be examined to see if they have any complications reported at their post-operative visits or any readmissions to the hospital. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT02741531
Study type	Interventional
Source	George Washington University
Contact
Status	Completed
Phase	N/A
Start date	March 2016
Completion date	July 27, 2017

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
Terminated	`NCT00551785` - Surveillance Study of Women Taking Intrinsa®	Phase 4
Completed	`NCT00528177` - Morphine vs. Oxycodone for Postoperative Pain Management	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

Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.

Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.

The Effect of Partial Bladder Filling on Post-operative Time to Void in Minimally Invasive Gynecologic Procedures

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms