Actively Recruiting

Phase 4
Age: 30Years - 100Years
All Genders
Healthy Volunteers
NCT05805436

Preop Laxatives in Robotic Urologic Surgery

Led by Chad R. Tracy · Updated on 2025-05-30

240

Participants Needed

1

Research Sites

143 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Minimally-invasive surgery, either laparoscopic or robotic, is commonly used in urology. Several urologic procedures including prostatectomy, radical nephrectomy, and partial nephrectomy are now commonly performed robotically. Patients undergoing these procedures often have delayed return of bowel function and persistent gastrointestinal symptoms including nausea/vomiting, abdominal distension, and bloating for several days to weeks after surgery. Postoperative stool softeners and laxatives are routinely used in an effort to minimize these symptoms, with varying degrees of success. The aim of this study will be to evaluate whether the use of a preoperative osmotic laxative will be beneficial in improving recovery of bowel function and alleviating postoperative gastrointestinal complaints in patients undergoing these procedures. Patients will be randomized to either receive or not receive three days of polyethylene glycol (PEG, also known as MiraLAX) on the three days before surgery. Patients in both groups will receive the same postoperative bowel regimen including scheduled PEG both in the hospital and upon discharge until first bowel movement. Patients will be given a questionnaire and diary to record their postoperative gastrointestinal symptoms and time to first bowel movement. These questionnaires and diaries will then be analyzed to determine differences in time to first bowel movement and gastrointestinal complaints during their recovery from surgery.

CONDITIONS

Official Title

Preop Laxatives in Robotic Urologic Surgery

Who Can Participate

Age: 30Years - 100Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients 30 years or older undergoing robotic-assisted laparoscopic radical prostatectomy, transperitoneal radical nephrectomy, or transperitoneal partial nephrectomy
Not Eligible

You will not qualify if you...

  • Patients under 30 years old
  • Patients with a contraindication to receiving polyethylene glycol or other forms of laxatives
  • People who regularly take Miralax
  • Patients undergoing retroperitoneal radical or partial nephrectomy
  • Patients with severe ulcerative colitis or Crohn's disease
  • Patients with intestinal diversions (colostomy, ileostomy)
  • Patients with prior abdominal or pelvic radiation
  • Patients who will not follow up with UIHC postoperatively
  • Patients who are incarcerated

AI-Screening

AI-Powered Screening

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Trial Site Locations

Total: 1 location

1

University of Iowa Hospitals & Clinics

Iowa City, Iowa, United States, 52242

Actively Recruiting

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Research Team

C

Chad Tracy, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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