The Effect of Solifenacin on Post Void Dribbling in Women

University of Wisconsin (UW)

Status: Completed

Conditions: Post-micturition Incontinence; Incontinence

Treatments: Drug: solifenacin

Study type: Interventional

Funder types: Other

Identifiers

NCT01470001

2011-0513

Details and patient eligibility

About

This is a double-blind, randomized, controlled, parallel design (n=140) study with the purpose of measuring the efficacy of Solifenacin 5mg in the treatment of women with Post Void Dribbling.

Full description

This investigation will have a double-blind, randomized, and controlled, parallel design with the % reduction in post void dribbling episodes (events) as the primary endpoint.

Secondary endpoints will include:

1. The % of patients with at least a 50% reduction in post void dribbling episodes.
2. Patient's perspective of the impact of their disease, which will be captured using the Pelvic Floor Distress Inventory, and another questionnaire that asks about urinary symptoms and quality of life.

We will compare Solifenacin 5 mg to placebo. 140 subjects will be enrolled, with 70 subjects in each arm. The treatment group will receive 5mg of Solifenacin daily for 12 weeks. Astellas Pharma will be supplying both drug and placebo, they will be prepackaged and numbered. The Pharmaceutical Research Center will randomly assign subjects into the treatment vs. placebo group blinding both the subjects and investigators

Enrollment: 118 patients

Sex: Female

Ages: 18 to 89 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

1. Women between the ages of 18 and 89
2. Incontinence in the form of post void dribbling that occurs at least twice weekly.

Exclusion criteria

1. Severe renal or hepatic disease.
2. Active urinary tract infection.
3. Glaucoma.
4. Stress incontinence as the only incontinence symptom
5. Urge incontinence as the only incontinence symptom
6. Chronic severe constipation.
7. History of bladder cancer.
8. Known or suspected hypersensitivity to anticholinergics.
9. Any clinical condition that would not allow safe completion of the study.
10. Pregnancy or lactation, intention to become pregnant during the study, or use of an unreliable birth control method in women of childbearing potential. Reliable forms of contraception include: permanent sterilization of either partner, hormonal contraception (oral contraceptive, Nuva ring, contraceptive patch, depoprovera, implants), intrauterine device (IUD), and condoms. Abstinence is considered a reliable form of contraception, but abstinent subjects will be informed that they need to use condoms or other form of birth control mentioned above if they become sexually active during the study.
11. Presently on systemic anti-cholinergic therapy or who have been on therapy within the last 4 weeks. Anti-cholinergic drugs include; darifenacin, fesoterodine, hyoscyamine, oxybutynin, solifenacin, tolterodine, and trospium.
12. Solid forms of potassium supplementation, as this presents an increased risk of GI side effects.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Double Blind

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118 participants in 2 patient groups, including a placebo group

solifenacin

Active Comparator group

Description:

patients in this arm will receive drug

Treatment:

Drug: solifenacin

placebo

Placebo Comparator group

Description:

patients is this arm will receive placebo

Treatment:

Drug: solifenacin