Comparing Immediate Removal and Postoperative 1 Day of Urinary Catheter After Colorectal Cancer Surgery
Enrolling by invitation · Not applicable
Conditions studied: Colorectal Cancer, Postoperative Complication, Urinary Retention Postoperative, Enhanced Recovery After Surgery
In brief
The enhanced recovery after surgery (ERAS) program is widely applied in colorectal cancer surgery. Among the early recovery programs after surgery, the timing of removal of the urinary catheter after surgery has been emphasized recently, but the specific timing is still under discussion. Maintaining the urinary catheter after surgery is to prevent urinary retention after surgery, but it is known that the risk of urinary tract infection increases the longer it is maintained. Previously, it was removed 3 days after colorectal cancer surgery, but several studies reported that even if it was removed earlier, the incidence of urinary retention did not increase, and rather the incidence of urinary tract infection decreased. In particular, by applying the early recovery program after surgery, factors related to patient recovery before, during, and after surgery are applied to help rapid recovery, and it has been reported that early removal of the urinary catheter has a positive effect on postoperative recovery and complications. Therefore, it is necessary to prove that the timing of removal of the urinary catheter after surgery in colorectal cancer patients can help early recovery through clinical results such as patient recovery and occurrence of complications.
Key facts
- Study ID
- NCT06769087
- Run by
- Seoul St. Mary's Hospital
- People needed
- 316
- Starts
- 2024-12-01
- Expected to finish
- 2026-12-31
- Last updated by the study team
- 2026-07-09
Who can join
Age: 19 and older, up to 80. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- 19 years old 80 years old
- Patients diagnosed with colorectal cancer who are eligible for radical resection surgery
- Patients who underwent open, laparoscopic, or robotic surgery
- Written informed consent
You may not qualify if…
- Patients who have undergone two or more major abdominal surgeries, including lateral pelvic lymph node dissection, at the same time
- Patients who require continuous monitoring through a urinary catheter due to hemodynamic instability or massive bleeding, etc.
- Patients who have undergone conventional treatment in cases other than distant metastasis or R0 resection
- Patients who have developed complications related to the urinary system during surgery and require maintenance of a urinary catheter such as a urethral stent
- Patients who have undergone urinary surgery such as urethral stent placement, cystectomy, or urostomy in the past
- Patients who are on hemodialysis or peritoneal dialysis due to chronic renal failure
- Patients who cannot participate in a clinical trial at the discretion of a physician
- Patients who do not wish to participate in the study
Where it is running
- Seoul St.Mary's hospital, the Catholic university of Korea — Seoul, Seoul, South Korea
Full record on ClinicalTrials.gov
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