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Early Post-operative Removal of Urethral Catheter in Patients Undergoing Colorectal Surgery With Epidural Analgesia

U

University College Hospital Galway

Status

Completed

Conditions

Urinary Retention

Treatments

Other: Removal of urethral catheter

Study type

Interventional

Funder types

Other

Identifiers

NCT01508767
Joyce-2011

Details and patient eligibility

About

Patients undergoing colon or rectal surgery will usually have a urinary catheter (silicone tube) placed in the bladder at the time of operating to monitor kidney function during surgery and in the post-surgery period. Such patients will also have an infusion into the spine, known as an epidural, after surgery to provide them with continuous pain relief. Urinary catheters should be removed as early as possible once they are no longer required to facilitate patients becoming mobile after surgery and to reduce the risk of patients developing a urinary tract infection.

Traditionally these catheters are not removed until the patients epidural infusion is withdrawn, as in theory to do so would predispose the patient to developing acute retention of urine due to lack of sensation when the bladder is full. The investigators hypothesis is that urinary catheters placed via the urethra can be withdrawn 48 hours after colon/rectal surgery in patients receiving epidural pain relief without a significant increase in rates of urinary retention.

Full description

Patients undergoing colon or rectal surgery will be randomly assigned to one of two groups: Patients in study group 1 (SG1) will have their urinary catheters removed at 48 hours post-operatively; Patients in study group 2 (SG2) will have their urinary catheters removed only after the epidural has been withdrawn in the post-operative period. We will be primarily examining rates of urinary retention in both groups. We will also be examining rates of urinary tract infection, chest infection (frequently a result of poor mobility after surgery), and wound infection and other complications after surgery.

Enrollment

41 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age > 18
  • Competent to consent to participate in trial
  • Undergoing colorectal surgery (any resection of large bowel, formation of colostomy, anterior resection, low anterior resection, panproctocolectomy, abdominoperineal resection).
  • Receiving epidural analgesia post-operatively
  • If male, international prostate symptom score <20.

Exclusion criteria

  • Previous lower urinary tract surgery
  • Chronic lower urinary tract disease
  • Intermittent self-catheterisation
  • Neurogenic bladder
  • Urethral catheter inserted >24 hours pre-operatively
  • Presence of pelvic sepsis/abscess at surgery
  • Previous trans-abdominal pelvic surgery
  • Urethral catheter required for urine output monitoring beyond 24 hours post-operatively
  • Presence of enterovesical fistula
  • Pre-operative use of medications which alter detrusor function
  • Pregnancy

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

41 participants in 2 patient groups

Study group 1
Experimental group
Description:
Early removal of urethral catheter 48 hours post-operatively.
Treatment:
Other: Removal of urethral catheter
Study group 2
Other group
Description:
Removal of urethral catheter once epidural analgesia has been withdrawn.
Treatment:
Other: Removal of urethral catheter

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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