What is the Optimal Technique for Hydrodistention?
Interstitial Cystitis, Bladder Pain Syndrome
About this trial
This is an interventional treatment trial for Interstitial Cystitis focused on measuring Hydrodistension
Eligibility Criteria
Inclusion Criteria:
- Patients with IC/BPS who have failed first/second line treatments (behavioral therapy, medications) for greater than 3 months
- Have not had hydrodistention performed in the past 3 months
- Have not had botox or Percutaneous tibial nerve stimulation (PTNS) performed in the past 3 months
Exclusion Criteria:
- Patients with known hunner's lesions
- Patients with interstim
- Patients with positive urinalysis/culture consistent with urinary tract infection (UTI)
- History of urethral, bladder, prostate, uterine, cervical, vaginal cancer
- History of augmentation cystoplasty or cystectomy
- History of urethral diverticulum, urethral stricture, pelvic radiation
- Patients with spinal cord injuries
- History of dementia, parkinson's disease, multiple sclerosis, spina bifida, paraplegia/quadriplegia, cerebral palsy, stroke
- Neurogenic bladder patients
- Anuric patients
- Tuberculous cystitis
- Cyclophosphamide treatment
- Pregnant patients
Sites / Locations
- University of Michigan
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Arm 5
Arm 6
Arm 7
Arm 8
Experimental
Experimental
Experimental
Experimental
Experimental
Experimental
Experimental
Experimental
Pressure (30 centimeters), Duration (1 minute), Number of times done (1)
Pressure (30 centimeters), Duration (2 minute), Number of times done (1)
Pressure (30 centimeters), Duration (1 minute), Number of times done (2)
Pressure (80 centimeters), Duration (1 minute), Number of times done (1)
Pressure (80 centimeters), Duration (2 minute), Number of times done (1)
Pressure (80 centimeters), Duration (1 minute), Number of times done (2)
Pressure (30 centimeters), Duration (2 minute), Number of times done (2)
Pressure (80 centimeters), Duration (2 minute), Number of times done (2)