Assessment of Patient-reported Goal Attainment in the Treatment of Female Overactive Bladder

NCT ID: NCT00836381

Last Updated: 2013-05-30

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE4
• Total Enrollment: 56 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2009-02-28
• Study Completion Date: 2012-01-31

Brief Summary

For many years, antimuscarinics have been first-line pharmacological treatment for OAB. A recent meta-analysis of randomised, controlled trials on antimuscarinic treatment of OAB concluded that the drugs provide significant improvements in OAB symptoms compared with placebo but that the benefits are of limited clinical significance. The analysis questioned the clinical significance of the trial results, one reason for which was the lack of data on the use of sensitive patient-driven criteria. Traditional symptomatic and urodynamic measures of treatment success may be meaningful to clinicians but often have little meaning to patients. Therefore, patient-reported outcomes (PROs), which provide a subjective measure of a patient's response to treatment, are useful. Recently, clinicians treating OAB have begun to recognize the value of PROs but still overlook the treatment efficacy in terms of patient-reported goal achievement (PGA).

Patients with OAB have combination of symptoms and the extent to which individual OAB symptoms affect patients varies. Also each patient can have different goal for the treatment. Therefore, assessing the degree of goal achievement in each patient can provide a new aspect of treatment benefit.

This controlled study will advance the understanding of OAB in terms of patient-centered treatments goals and goal achievement and will provide a new aspect of treatment benefit.

Detailed Description

1. Objectives

1. Primary objective: To explore the "Patient-reported Goal Attainment (PGA)" after 12 weeks of treatment with tolterodine extended-release (ER) 4mg in female overactive bladder (OAB) patients.

2. Secondary objective: To explore the patient-reported treatment goals and the efficacy of tolterodine on the patient-reported outcomes (PROs), micturition diary parameters, and safety parameters from baseline to 12 weeks of treatment in female OAB patients.

2. Specific aim

: To compare the efficacy of tolterodine ER 4mg with that of placebo, on PROs in terms of PGA after 12 weeks of treatment in female OAB patients.

3. Experimental/research design

1. 12-week randomized, placebo-controlled, double-blind, parallel-group, prospective study in Korean women with symptoms of OAB

2. Treatment: Each patient will receive tolterodine ER (4 mg, qd) or placebo (randomized in the ratio of 1:1) for 12 weeks.

3. Time schedule Start date: 01/Jan/2009 Finish date: 01/Sep/2009 Duration of washout: 7 days Duration of run-in: 7 days Duration of enrollment period: 5 months Duration of treatment period: 12 weeks Completion of analysis: 6 weeks

Conditions

Overactive Bladder

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: TRIPLE

Study Groups

Tolterodine ER

Tolterodine ER 4mg once daily

Group Type: EXPERIMENTAL

Tolterodine extended-release (ER) 4mg

Intervention Type: DRUG

Tolterodine extended-release (ER) 4mg once daily for 12 weeks

Placebo

Placebo once daily

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: DRUG

Identical Placebo once daily

Interventions

Tolterodine extended-release (ER) 4mg

Tolterodine extended-release (ER) 4mg once daily for 12 weeks

Intervention Type: DRUG

Placebo

Identical Placebo once daily

Intervention Type: DRUG

Other Intervention Names

Detrusitol ER 4mg

Eligibility Criteria

Inclusion Criteria

1. Female aged ≥ 18 and ≤ 80 years

2. Symptoms of OAB as verified by the screening 3 day micturition diary, defined by:

Mean urinary frequency ≥8 times/24 hours Mean number of urgency episodes ≥ 2 episode/24 hours

3. Symptoms of OAB for ≥ 3 months.

4. Ability and willingness to correctly complete the micturition diary and questionnaire

5. Capable of understanding and having signed the informed consent form after full discussion of the research nature of the treatment and its risks and benefits

Exclusion Criteria

1. Subjects with stress incontinence or mixed stress/urge incontinence where stress incontinence is the predominant component based on prior history.

2. Significant hepatic or renal disease, defined as having twice the upper limit of the reference range for serum concentrations of aspartate amino- transferase (AST [SGOT]), alanine aminotransferase (ALT [SGPT]), alkaline phosphatase or creatinine.

3. Any condition that is a contraindication for anticholinergic treatment, including uncontrolled narrow-angled glaucoma, urinary retention or gastric retention

4. Symptomatic acute urinary tract infection (UTI) during the run-in period

5. Recurrent UTI defined as having been treated for symptomatic UTI > 4 times in the last year

6. Diagnosed or suspected interstitial cystitis

7. Clinically significant bladder outlet obstruction or poor detrusor function defined by clinical symptoms and investigator's opinion according to local standard of care

8. Previous history of major urethral and/or bladder surgery

9. History of radiation treatment (external or interstitial) to pelvic organs or external genitalia for any reason.

10. Subjects with neuropathology that could affect the lower urinary tract or nerve supply

11. Patients with marked cystocele or other clinically significant pelvic prolapse.

12. Subjects with current (within 2 years) urogenital neoplasms or malignancies including bladder, uterine or cervical cancer

13. Treatment within the 14 days preceding randomization, or expected to initiate treatment during the study with: Any anticholinergic drugs other than trial drug Any drug treatment for overactive bladder

14. On an unstable dosage of any drug with anticholinergic side effects, or expected to start such treatment during the study

15. Subjects currently taking tricyclic antidepressants, diuretics or alpha blockers who have not been on a stable dose of these medications for at least one month

16. Current administration of a selective serotonin reuptake inhibitor (SSRI) and has not been on a stable dose for at least three months

17. Receipt of any electrostimulation or bladder training within the 14 days before randomization, or expected to start such treatment during the study

18. An indwelling catheter or practicing intermittent self-catheterization

19. Use of any investigational drug within 1 months preceding the start of the study

20. Patients with chronic constipation or history of severe constipation

21. Pregnant or nursing women

22. Sexually active females of childbearing potential not using reliable contraception for at least 1 month prior to study start and not agreeing to use such methods during the entire study period and for at least 1 month thereafter *Reliable contraceptive methods are defined as intrauterine devices (IUDs), combination type contraceptive pills, hormonal implants, double barrier method, injectable contraceptives and surgical procedures (tubal ligation or vasectomy).

23. Any other condition which makes the patient unsuitable for inclusion.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 80 Years
• Eligible Sex: FEMALE
• Accepts Healthy Volunteers: No

Sponsors

Pfizer

INDUSTRY

Sponsor Role: collaborator

Samsung Medical Center

OTHER

Sponsor Role: lead

Responsible Party

KYU-SUNG LEE

Proffesor

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

2008-09-006

Identifier Type: -

Identifier Source: org_study_id