Effects of terazosin and tolterodine on ureteral stent related symptoms: a
double-blind placebo-controlled randomized clinical trial.
Author(s): Tehranchi A(1), Rezaei Y, Khalkhali H, Rezaei M.
Affiliation(s): Author information:
(1)Department of Urology, Urmia University of Medical Sciences, Urmia, Iran.
Publication date & source: 2013, Int Braz J Urol. , 39(6):832-40
OBJECTIVE: To evaluate the effects of terazosin and tolterodine on ureteral stent
discomfort.
MATERIALS AND METHODS: Of 163 patients assessed for eligibility, 104 patients
were randomly assigned to receive placebo, 2 mg of terazosin twice daily, 2 mg of
tolterodine daily, or both terazosin plus tolterodine during the stenting period.
Prior to stenting and at stent removal, the International Prostate Symptom Score
(IPSS), the IPSS quality of life (QoL) subscore and the Visual Analog Scale for
Pain were determined. The patients also reported their analgesic use during the
stenting period.
RESULTS: Ninety-four patients completed the study. We noted significant decreases
in the total IPSS scores (p = 0.002), irritative subscore (p = 0.039), QoL (p =
0.001), flank pain (p = 0.013), voiding pain (p = 0.01) and amount of analgesics
used (p = 0.02) in the groups. However, neither the obstructive subscore nor the
suprapubic pain improved significantly (p = 0.251 and p = 0.522, respectively).
The patients receiving terazosin plus tolterodine experienced significant
reductions in the total IPSS, irritative symptoms, QoL, flank pain, voiding pain
and decreased analgesics use compared with those patients receiving placebo.
However, compared with placebo, terazosin monotherapy did not affect pain levels,
and tolterodine monotherapy did not improve QoL, flank pain or analgesics use.
CONCLUSIONS: Terazosin plus tolterodine improves ureteral stent-related
complications, including irritative symptoms, the amount of analgesics used, QoL,
flank pain and voiding pain but does not decrease obstructive symptoms or
suprapubic pain. This trial was registered at www.clinicaltrials.gov as
NCT01530243.
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