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- W2594119755 abstract "Patients with IC/BPS refractory to conventional treatment for at least 6 months were recruited in this study. All the subjects were randomized in a 2:1 ratio to receive hydrodistention plus intravesical suburothelial injection of BoNT-A 100 U (Botox group) or equivalent amount of normal saline (N/S group) in a 20 sites setting. Post-baseline study visits/assessments were conducted at weeks 2, 4 and 8. The primary endpoint was improvement of pain visual analogue scale (VAS). The secondary endpoints included changes in the O'Leary-Sant symptom index (ICSI) and problem index (ICPI), global response assessment (GRA), functional bladder capacity (FBC), frequency, nocturia, maximum flow rate (Qmax), voided volume (VV), post-void residual urine (PVR), and cystometry bladder capacity (CBC). Patients with Hunner's ulcer, PVR >150 ml or active urinary tract infection were excluded. An improvement of pain VAS >=2 or GRA >=1 was defined as treatment success. Safety was assessed by evaluating adverse events (AE)." @default.
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- W2594119755 date "2014-10-20" @default.
- W2594119755 modified "2023-09-28" @default.
- W2594119755 title "Therapeutic effects of intravesical onabotulinumtoxinA injection on IC/BPS refractory to conventional treatment - a randomized, double blind, placebo controlled study" @default.
- W2594119755 hasPublicationYear "2014" @default.
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