Skip to content

The efficacy of Choreito on female lower urinary tract symptoms with bladder pain

The evaluation of the efficacy and the safety of Choreito on female lower urinary tract symptoms with bladder pain

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCTs071190017
Enrollment
50
Registered
2019-08-01
Start date
2019-11-22
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Lower urinary tract symptom

Interventions

Choreito treatment

Sponsors

Takei Mineo
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Patient aged 20 to 90 Female patient with CLSS questionnaire Q9 (Bladder pain) 2 or higher Total IPSS score 8 or higher

Exclusion criteria

Exclusion criteria: Patient with serious cardiovascular, liver disease and renal dysfunction. Liver disease:Patients whose AST, ALT or both are more than three times the facility reference upper limit. Renal dysfunction:Creatinine are more than 2 times the facility reference upper limit. Woman who is pregnant, nursing, wishes to be come pregnant the study period, or can not follow instruction of physician regarding contraception. Patients who carried the radiation therapy to the pelvis. Patients with activity of urinary tract infection. Patients who have history of Kampo allergies. Other patients who are assessed to be inappropriate for study participation by the investigator.

Design outcomes

Primary

MeasureTime frame
Core Lower Urinary Tract Symptom Score(CLSS) Q9 (Bladder pain)

Secondary

MeasureTime frame
CLSS IPSS IPSS-QOL Severity criteria for interstitial cystitis Uroflowmetry Residual urine Record of urination Overall Treatment Efficacy Blood parameter (IFNg, High sensitive CRP)

Contacts

Public ContactFusami Shibata

Harasanshin Hospital

shibata.f@harasanshin.or.jp+81-92-291-3434

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026