Does Spinal Anesthesia for Prolapse Surgery With Lead to Urinary Retention?
Status unconfirmed · Not applicable
Conditions studied: Urinary Retention, Uterine Prolapse
In brief
The purpose of the study is to compare the risk of being unable to urinate shortly after surgery, also called acute post-operative urinary retention (POUR) between spinal and general anesthesia in women who undergo outpatient pelvic organ prolapse with stress urinary incontinence surgery.
Key facts
- Study ID
- NCT02547155
- Run by
- The Cleveland Clinic
- People needed
- 68
- Starts
- 2015-03-01
- Expected to finish
- 2017-12-01
- Last updated by the study team
- 2017-04-20
Who can join
Age: 40 and older. Sex: female. Healthy volunteers: accepted.
You may qualify if…
- Women over the age of 40
- Women scheduled for pelvic organ prolapse surgery as well as concomitant incontinence sling surgery
- Post-void residual <150 cc prior to surgery
- Surgery length of at least 1 hour
- BMI <40
- ASA class 1-2
You may not qualify if…
- Contraindications to surgery
- Contraindications to outpatient surgery, and requiring inpatient stay for medical comorbidities. The decision for a required inpatient stay will be decided prior to surgery based on the recommendations of the patient's primary care physician or specialist, such as cardiology or pulmonology.
- BMI >40
- ASA class 3 or 4 that would be a contraindiction to both spinal or general anesthesia
- Evidence of voiding dysfunction or urinary retention on pre-operative urodynamics, including PVR >150, or dyssynergic sphincter dyssynergia
- Neurological diseases that can interfere with spinal anesthesia
- Anticoagulation therapy within a week of surgery
- History of back surgery that would prevent successful spinal anesthesia
- History of back deformity, such as scoliosis that would prevent successful spinal anesthesia
Where it is running
- Cleveland Clinic Florida — Weston, Florida, United States (enrolling)
Full record on ClinicalTrials.gov
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