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Does Straight Catheterization in Short Gynecologic Procedures Cause Bacteriuria?

Intraoperative One-Time Catheterization in Short Gynecologic Procedures and Its Potential Effect on Symptomatic and Asymptomatic Bacteriuria

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01926756
Enrollment
200
Registered
2013-08-21
Start date
2013-07-31
Completion date
Unknown
Last updated
2013-08-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Postoperative Bacteriuria

Keywords

bacteriuria, straight catheterization, urinary tract infections, iatrogenic

Brief summary

This is a prospective randomized controlled trial to look into the reduction of catheter associated urinary tract infections in the postoperative period. It will specifically look at short gynecologic procedures such as D&C (dilation and curettage), hysteroscopies and LEEP procedures and the need to perform intraoperative catheterization. If a patient urinates immediately before a short operation then there is no need to drain the bladder with a catheter during the procedure. The investigators hypothesize that eliminating catheterization during these short procedures may decrease postoperative urinary tract infections. The hope is that this study would provide evidence to support a change in practice.

Detailed description

The majority of research currently concentrates on indwelling catheters rather than one-time catheterization. Current practice at our institution in the gynecologic operating room is to perform a one time catheterization on patient's undergoing short procedures, yet it is unclear if this is a necessary intervention. If patients are asked to void immediately before their procedure it would eliminate the need for intra-operative catheterization and eliminate a potential source of infection. The study is designed to determine whether routine catheterization prior to a minor OB/GYN procedure causes symptomatic or asymptomatic bacteria in the urine. Current practice is one-time catheterization of patients undergoing minor OB/GYN procedures prior to the beginning of the procedure. The investigators hypothesize that this causes asymptomatic or symptomatic bacteriuria.

Interventions

PROCEDUREStraight catheterization

Patient will receive the current standard practice of straight catheterization intraoperatively.

PROCEDURENo straight catheterization

Patients will not be catheterized which is an experimental change from the current practice at our hospital.

Sponsors

Abington Memorial Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* The patient must be 18 years of age or older. * The patient must be female. * The patient must be undergoing a same-day gynecologic procedure where catheterization is usually performed. * The patient must have general anesthesia or monitored anesthesia care (MAC). This includes IV sedation.

Exclusion criteria

* The patient cannot be undergoing intermittent one-time catheterization. * The patient can not have had an indwelling catheter placed in the past 6 months. * The patients cannot have a concomitant pelvic infection. * The procedure cannot require spinal anesthesia. * The patient cannot be taking immunosuppressive medications. * The patient cannot be taking antibiotics and/or suppressive therapy for chronic urinary tract infections. * The patient cannot receive pre-operative or intra-operative antibiotics.

Design outcomes

Primary

MeasureTime frameDescription
Postoperative Bacteriuria2 -4 weeksUrine cultures are obtained preoperatively (baseline), immediately postoperatively and 2 to 4 weeks postoperatively.

Secondary

MeasureTime frame
Subjective urinary tract discomfort2-4 weeks postoperatively

Other

MeasureTime frame
Symptomatic urinary tract infection2-4 weeks

Countries

United States

Contacts

Primary ContactEmily G Parent, D.O.
eparent@amh.org215-481-7663
Backup ContactVictoria Myers, M.D.
vmyers@amh.org215-481-8379

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026