← Back to all trials
Not Yet Recruiting
NCT05617118
BTA vs Baclofen for Pelvic Myofascial Pain Syndrome
Conditions: Chronic Pain, Chronic Pelvic Pain Syndrome, Myofascial Pain Syndrome, Myofascial Trigger Point Pain, Pelvic Floor Disorders
Sex: All
Ages: 18 Years – 75 Years
Enrollment: 52
Sponsor: Saint Petersburg State University, Russia
Summary
The aim of the study is to test the hypothesis that oral taking of baclofen in therapeutic dosage for 60 days is equally effective as injection of botulinum toxin type "A" in the area of trigger points of the pelvic muscles.
Eligibility Criteria
Inclusion Criteria:Myofascial pain syndrome (presence of trigger points), confirmed by palpation during examination.Ineffectiveness (with subsequent discontinuation) of at least one treatment method, including outpatient physiotherapy and /or oral analgesics, or NSAIDs.Exclusion Criteria:The presence of any organic disease of the pelvic organs requiring active treatment, confirmed by anamnesis, consultation of a specialist (urologist, proctologist, gynecologist) and one of the objective imaging methods: CT, MRI, endoscopical or laboratory methods: general urine analysis or prostate secretion analysis.
Such diseases include interstitial cystitis / SBMP, chronic prostatitis types I, II, IIIA according to the NIH classification.The presence in the anamnesis of the fact of previously conducted therapy with baclofen or injection of botulinum toxin type "A" into the pelvic floor muscles.Individual intolerance to botulinum toxin type "A" and /or baclofen.Pregnancy
Source: ClinicalTrials.gov (NCT05617118). StuddyBuddy aggregates publicly available trial information.