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Search / Trial NCT05805436

Preop Laxatives in Robotic Urologic Surgery

Launched by CHAD R. TRACY · Mar 22, 2023

Trial Information

Current as of June 26, 2025

Recruiting

Keywords

ClinConnect Summary

This clinical trial is studying whether taking a specific type of laxative called polyethylene glycol (PEG, also known as MiraLAX) before surgery can help patients recover better from robotic urologic procedures, such as surgeries for prostate or kidney cancer. Many patients experience issues like nausea, bloating, and difficulty having bowel movements after surgery, which can delay their recovery. In this trial, some patients will take the laxative for three days before their surgery, while others will not. All participants will follow the same plan for bowel care after surgery, and they will keep track of their symptoms and when they have their first bowel movement.

To be eligible for this study, patients need to be at least 30 years old and scheduled for certain robotic-assisted surgeries. They cannot have certain health conditions or take laxatives regularly. Participants will be asked to complete questionnaires and keep a diary about their recovery, which will help researchers understand if taking the laxative beforehand makes a difference in their recovery experience. This study is currently looking for volunteers and aims to improve the overall recovery process for patients undergoing these types of surgeries.

Gender

ALL

Eligibility criteria

  • Inclusion criteria:
  • -Patients 30 years or older undergoing robotic-assisted laparoscopic radical prostatectomy, transperitoneal radical nephrectomy, or transperitoneal partial nephrectomy
  • Exclusion criteria:
  • 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

About Chad R. Tracy

Chad R. Tracy is a dedicated clinical trial sponsor with a commitment to advancing medical research and improving patient outcomes. With extensive experience in trial design and management, Tracy focuses on innovative therapies and evidence-based practices across various therapeutic areas. His approach emphasizes collaboration with healthcare professionals, regulatory bodies, and research institutions to ensure the highest standards of ethics and compliance. By fostering a patient-centric environment, Chad R. Tracy aims to deliver meaningful contributions to the medical community and address unmet clinical needs through rigorous research and development initiatives.

Locations

Iowa City, Iowa, United States

Patients applied

0 patients applied

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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