Prospective Study for Patient Perception of Treatment Satisfaction After Switching to Mirabegron in Patients With Overactive Bladder Who Were Unsatisfied With Efficacy of Antimuscarinic Therapy or Adverse Event.

NCT ID: NCT02468375

Last Updated: 2018-02-28

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE4
• Total Enrollment: 434 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2015-06-30
• Study Completion Date: 2017-12-31

Brief Summary

The purpose of this study is to measure the treatment satisfaction after switching to mirabegron in patient with Overactive Bladder(OAB) who were unsatisfied with efficacy of antimuscarinic therapy or adverse event.

Patient will take the mirabegron 50mg/day for 12 weeks, and the satisfation of the therapy will be measured with Treatment Satisfaction Questionnaire(TSQ), Global Response Assessment(GRA), OAB-q short form, OAB Symptom Score and Willingness to continue Questions.

Conditions

Overactive Bladder

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

mirabegron 50mg

about 434 OAB patients intake mirabegrone 50mg/day for 12 weeks.

Group Type: EXPERIMENTAL

mirabegron 50mg

Intervention Type: DRUG

434 OAB patient intake mirabegron 50mg/day for 12 weeks.

Interventions

mirabegron 50mg

434 OAB patient intake mirabegron 50mg/day for 12 weeks.

Intervention Type: DRUG

Other Intervention Names

Betamiga tablet

Eligibility Criteria

Inclusion Criteria

<SCREENING>

1. over 20 years old, who has overactive bladder at least for 3 months.

2. total OABSS score over 3 points, and number 3 question score should be over 2 points.

3. if one of the criteria met,

1) efficacy : who are unsatisfied with antimuscarinics during the past 2 years. (should be treated at least 8 weeks) 2) adverse event(AE) : who are unsatisfied with antimuscarinics treatment due to AE(dry mouth, constipation, etc) 4.subject who can write voiding diary. 5.subject who can understand about the study and sign the informed concent form.

<BASELINE> Voiding Diary for 3 days

1. micturition 8/day

2. urgency 2/day

Exclusion Criteria

<SCREENING>

1. subject has history or risk of acute urinary retension.

2. subject has prostate cancer.

3. subject has lower urinary tract obstruction and judge by investigator that the subject is not appropriate to participate in this study.

4. subject has a previous or current bladder tumor.

5. subject has significant stress incontinence or mixed incontinence where stress is the dominant factor.

6. prohibitied, permitted medication. 6-1. subject who has intake Alpha-blocker, Diabetes insipidus medication, PDE5 inhibitor(for BPH Tx), SSRI within 12weeks prior to Screening.

6-2. subject who has started, stopped or changed the dose of 5-Alpha Reductase Inhibitors(5-ARI) within 4 weeks prior to Screening.

6-3. Subject who currently intake Antimuscarinics, Antihistamines, Beta 2-adrenoreceptor agonist, loop diuretics,CYP2D6 substrates with narrow therapeutic index, CYP3A4 inducing agent, CYP 3A4 inhibitor, Antifungal agent, Antiarrythmic drugs.

7. subject who has Non-drug treatment including bladder training, pelvic floor muscle training within 12 weeks prior to Screening.

8. subject has severe hypertension which is defined as a sitting average systolic blood pressure over 180 mmHg, and/or diastolic blood pressure over 11 0mmHg.

9. pulse over 100 bpm or below 50 bpm.

10. subject has an indwelling catheter or practices intermittent self-catheterization.

11. subject who had surgery which can influence urinary track function (ex, TURP, Laser treatment,etc.).

12. subject who had complication of urinary tract infection, urinary stone, interstitial cystitis, or recurrent UTI history.

13. subject has known or suspected hypersensitivity to Beta 3 adrenalin receptor agonist.

14. subject has clinically significant cardiovascular diseases hepatic diseases renal diseases immunization diseases lung diseases and cancer.

15. subject who has planed pregnency, breast feeding during clinical trial period.

<BASELINE> voiding volume over 3000ml per day. post voiding residual volume over 200ml

• Minimum Eligible Age: 20 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Samsung Medical Center

OTHER

Sponsor Role: lead

Responsible Party

KYU-SUNG LEE

professor

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Kyu-Sung Lee, Ph.D

Role: PRINCIPAL_INVESTIGATOR

Samsung Medical Center

Locations

Samsung Medical Center

Seoul, , South Korea

Countries

South Korea

Other Identifiers

2015-02-052

Identifier Type: -

Identifier Source: org_study_id