Impact of Integrated Care Pathways for Prevention of Post-operative Urinary Retention (POUR)
Status unconfirmed · Not applicable
Conditions studied: Arthroplasty, Replacement, Hip, Arthroplasty, Replacement, Knee, Urinary Retention
In brief
A prospective randomized control trial will be conducted at Good Samaritan Hospital and TriHealth Evendale Hospital. Subjects will receive total hip or knee surgery and follow-up via standard care at the discretion of the treating physician or the experimental study arm in which all patients will undergo the integrated care pathway.
Key facts
- Study ID
- NCT03863743
- Run by
- TriHealth Inc.
- People needed
- 164
- Starts
- 2019-02-05
- Expected to finish
- 2022-02-05
- Last updated by the study team
- 2021-03-01
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- ASA grade I- III
- BMI under 36 kg/m\^2
- Scheduled surgery for primary total hip or knee replacement
- Age 18+ years
You may not qualify if…
- Contraindications or failure of neuraxial anesthesia
- Patients must not be outpatient total hip or knee procedure
- Known intercurrent UTI, incontinence, or urinary retention not addressed by pre-operative urologic consultation and correction
- Pregnancy
- Current nicotine, alcohol or drug abusers
- Pre-operative narcotic use (any narcotic consumption within 3 days prior to surgery)
- Post- operative parenteral narcotic administration
- Allergy or intolerance to liposomal bupivacaine, bupivacaine, celecoxib, dexamethasone and/or pregabalin
Where it is running
- TriHealth Good Samaritan Hospital — Cincinnati, Ohio, United States (enrolling)
- TriHealth Evendale Hospital — Cincinnati, Ohio, United States (enrolling)
Full record on ClinicalTrials.gov
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