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The study will employ 4 treatment arms and 1 placebo arm to compare efficacy of CBT, PFT, Pharmacotherapy, Integrated CBT and PFT modalities in the management of chronic pelvic pain in women.
Enrollment
Sex
Ages
Volunteers
Inclusion criteria
Women of reproductive age, Women with CPP having no pathological or anatomical causes, Women with Overactive Bladder Syndrome Women with Vulvodynia.
Exclusion criteria
Women experiencing per-menopause or menopause, Women with medical, or gynecological or hormonal abnormalities, Women with mental disorders, Women who use substances.
Primary purpose
Allocation
Interventional model
Masking
40 participants in 5 patient groups, including a placebo group
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Data sourced from clinicaltrials.gov
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