Urinary Retention
Conditions
Brief summary
This is a prospective, comparative randomized study. Our study population includes women with pelvic organ prolapse undergoing a robotic assisted laparoscopic sacrocolpopexy. The two groups will include the study group, who will have their Foley catheter removed 6 hours post-op, and the control group who will have an indwelling Foley catheter overnight. The two groups will be assigned according REDCap randomization system.
Interventions
OTHERNo Foley
Patients will have Foley catheter removed 6 hours post-op.
Sponsors
Atlantic Health System
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE
Eligibility
Sex/Gender
FEMALE
Age
19 Years to 75 Years
Healthy volunteers
Yes
Inclusion criteria
* Age 19-75 * Pelvic organ prolapse requiring robotic assisted, laparoscopic sacrocolpopexy.
Exclusion criteria
* Intraoperative complications necessitating a post-operative Foley * Cystotomy * EBL \>500mL * Bowl injury * Pre-operative urinary retention requiring an indwelling catheter
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Urinary retention | 6 hours after discharge from PACU | Patients in the intervention group will have their Foley catheter removed up to 6 hours after discharge from the PCA. They will then have to undergo a voiding trial |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Urinary Tract Infections | 30 day post op | All UTIs will be documented up to 30days post op. |
| Post-operative complications | 30 days post op | Post-operative complications |
Countries
United States
Outcome results
None listed