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Study selection Study inclusion criteria were as follows: patients diagnosed with IC/BPS, interventions included relevant treatments, comparisons were specified as control or placebo, outcomes were mean differences for individual symptoms (pain, frequency, urgency and nocturia) and structured questionnaires (ICPI, ICSI, PUF and FBV) using an RCT study design
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The recovery timeline primarily depends on factors such as the deficiencys severity and duration, the presence of neurological symptoms, and any absorption issues
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