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Control of chronic nonbacterial prostatitis symptoms

Phase 2
Conditions
Chronic nonbacterial prostatitis.
Chronic prostatitis
Registration Number
IRCT2016071025507N4
Lead Sponsor
Vice Chancellor for Research of Arak University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Male
Target Recruitment
116
Inclusion Criteria

Age over 18 years; no prior history of other urinary system disorders such as urinary tract stones, neurogenic bladder, and urinary infections; no history of underlying diseases such as cirrhosis, renal failure, diabetes, or hypertension; normal levels of urine, fasting blood sugar (FBS), and creatinine; normal results on the first neurological examination of the perineal area, lower limbs, lower limb reflexes, and bulbocavernosus reflex; having weight between 50 to 100 kg; no use of other medicines; no signs of psychological disorders; confirmed diagnosis of chronic prostatitis; creatinine equal to or lower than 1.2 mg; platelet count over 100000/mm3; non-sensitivity to anti-epileptic drugs, pregabalin, thiazolidinediones, or other anti-diabetic agents.
Exclusion criteria: Unwillingness to continue the study; major side-effects due to the use of medications.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain scale. Timepoint: Two, four and six weeks after intervention. Method of measurement: NIH-CPSI and GRA questionnaire.
Secondary Outcome Measures
NameTimeMethod
Side-effects of pharmaceuticals including nausea, vomiting, hypotension, itching and drowsiness. Timepoint: Two, four and six weeks after intervention. Method of measurement: Questionnaire.
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