Interstitial Cystitis/Bladder Pain Syndrome (IC/BPS). Interstitial Cystitis/Bladder Pain Syndrome (IC/BPS)
Conditions
Interventions
Intervention group: Protokin therapy. 10 cc of blood is taken from the patient (using a protokine syringe) and incubated at 37 oc for 6-9 hours and centrifuged at 5000 rpm for 6 minutes. Finally, 4.5
Sponsors
Tabriz University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: All patients with painful bladder syndrome/interstitial cystitis who were resistant to first, second and third line treatment (Botox injection). Patients who had urodynamic evaluation before injection
Exclusion criteria
Exclusion criteria: Lack of consent to participate in the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| BPIC-SS questionnaire scores. Timepoint: Before and 1 and 3 months after injection. Method of measurement: BPIC-SS questionnaire.;Determining the level of patients' satisfaction with the intervention. Timepoint: Before and 1 and 3 months after injection. Method of measurement: Based on the evaluation checklist, the patient's satisfaction with the procedure is measured from completely satisfied to completely dissatisfied: the evaluated questions include: completely satisfied, somewhat satisfied, dissatisfied, completely dissatisfied.;Determining the amount of side effects in patients. Timepoint: 1 and 3 months after injection. Method of measurement: Checklist for any side effects. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactSakineh hajebrahimi
Tabriz University of Medical Sciences
Outcome results
None listed