Urinary Retention Clinical Trial
Official title:
Prospective Study Investigating Optimal Duration of Indwelling Urinary Catheter Following Infraperitoneal Colorectal Surgery and Role of Postoperative Alpha Blockade
Verified date | January 2019 |
Source | Cedars-Sinai Medical Center |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
There is no general agreement about the optimal duration of postoperative urinary drainage, with relevant literature reporting durations ranging from 1 to 10 days. The available research supporting the routine use of prolonged catheterization is limited and studies investigating early removal following infraperitoneal colorectal surgery have largely been underpowered to form valid practice conclusions. The aim of the investigators study is to determine whether a postoperative colorectal patient can safely have an indwelling catheter removed on postoperative day one (24 hours following surgery) with the addition of a study medication (prazosin), without a statistically significant difference in the incidence of urinary retention compared to the standard, accepted approach of delayed removal (72 hours postoperatively). Patients undergoing laparoscopic and open pelvic colorectal surgery below the peritoneal reflection for both benign and malignant conditions will be randomized into two groups: group one will have the catheter removed on postoperative day 3 (72 hours postoperatively) Group 2 will have a dose of the alpha-blocker prazosin given 6 hours prior to catheter removal and will have the urinary catheter removed on postoperative day 1 (24 hours postoperatively).
Status | Completed |
Enrollment | 142 |
Est. completion date | November 22, 2017 |
Est. primary completion date | November 22, 2017 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: 1. Able to freely give written informed consent to participate in the study and have signed the Informed Consent Form; 2. Males or females, >18 years of age inclusive at the time of study screening; 3. American Society of Anesthesiologists (ASA) Class I-III; 4. Infraperitoneal colorectal surgery (open and/or laparoscopic); 5. Elective Surgery Exclusion Criteria: 1. Mentally incompetent or unable or unwilling to provide informed consent or comply with study procedures; 2. Children <18; 3. No perioperative antibiotics; 4. Past or current urinary tract malignancy; 5. Urinary catheter inserted before surgery; 6. Chronic kidney insufficiency with Creatinine> 2 7. Diagnosis of benign prostatic hyperplasia 8. Chronic urinary infections 9. Neurogenic bladder 10. History of enterovesical fistula 11. Pregnancy 12. Prior surgery of the lower urinary tract 13. Epidural 14. Perioperative ureteral stents After randomization: 1. Catheter pulled out inadvertently; 2. Postoperative complications requiring prolonged monitoring of urine output 3. Postoperative complications requiring early reoperation |
Country | Name | City | State |
---|---|---|---|
United States | Cedars-Sinai Medical Center | Los Angeles | California |
Lead Sponsor | Collaborator |
---|---|
Cedars-Sinai Medical Center |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Number of Participants With Acute Urinary Retention | Acute urinary retention will be defined as catheter discontinuation with inability to void 6 hours post-removal, or void with post-void residual greater than 200 cc of urine. | Postoperative day 1 or postpoperative 3 depending on group randomization | |
Secondary | Number of Participants With a Symptomatic Urinary Tract Infection | Urinary tract infection defined as symptomatic urinary complaints such as dysuria, with urinalysis consistent with infection. | During 1 week of hospitalization (prior to discharge) |
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