A Phase 4 interventional study of solifenacin succinate (VESIcare) and placebo in Overactive Bladder in Parkinson's Disease, sponsored by University of South Florida. Completed at 3 sites in United States. Open to participants aged 40 Years to 80 Years. Per ClinicalTrials.gov, last updated 2021-11-09.
Sponsored by University of South Florida · Phase 4, Interventional, and Treatment
This study will assess the effectiveness of solifenacin succinate (VESIcare) in reducing symptoms of overactive bladder in Parkinson's disease (PD) patients.
4,487 studies on the registry are indexed under Parkinson Disease; 1,082 are open to participants now.
This study's enrollment of 23 is below the median of 40 across 3,294 interventional studies indexed under Parkinson Disease.
Browse Parkinson Disease studies →University of South Florida is the lead sponsor of 333 studies on the registry; 63 are open to participants now.
Of its 17 completed or terminated interventional studies of FDA-regulated products, 4 (24%) have results posted.
Counted across the registry records on this site, refreshed daily.
Exclusion Criteria:
Currently taking any of the following medications:
Drug: solifenacin succinate (VESIcare)
Drug: placebo
up to 10mg every day orally
placebo matching solifenacin succinate (VESIcare) up to 10mg orally every day
Number of Micturations Per 24 Hour Period
The primary objective of this study is to measure the efficacy of solifenacin succinate (VESIcare) in reducing the mean number of micturitions per 24 hour period in Parkinson's disease (PD) patients as measured by voiding diaries.
Time frame: 12 weeks
Number of Urinary Incontinence Episodes Per 24 Hour Period
This scale it the mean number of urinary incontinence episodes per 24 hour period, as assessed by a 3-day bladder diary. The goal is to examine the effect of solifenacin succinate (VESIcare) on urinary incontinence severity.
Time frame: 12 weeks
Unified Parkinson's Disease Rating Scale (UPDRS) Total
To examine the effect of solifenacin succinate (VESIcare) on Parkinson's disease severity. The UPDRS total score ranges from 0 (no disability) to 199 (total disability).
Time frame: 12 weeks
Parkinson's Disease Quality of Life Scale (PDQOL)
This scale is used to assess quality of life in Parkinson's Disease patients. Parkinson's disease quality of life scale has a possible point range from 37 (worst outcome) to 185 (best outcome). The goal of this outcome measure is to examine the effect of solifenacin succinate (VESIcare) on quality of life.
Time frame: 12 weeks
Number of Nocturia Episodes Per 24 Hour Period
To examine the effect of solifenacin succinate (VESIcare) on urinary incontinence severity
Time frame: 12 weeks
| Milestone | Solifenacin Succinate (VESIcare) | Placebo |
|---|---|---|
| Started | 10 | 13 |
| Completed | 9 | 12 |
| Not completed | 1 | 1 |
| Withdrew: Withdrawal by subject | 1 | 0 |
| Withdrew: Lost to follow-up | 0 | 1 |
The primary objective of this study is to measure the efficacy of solifenacin succinate (VESIcare) in reducing the mean number of micturitions per 24 hour period in Parkinson's disease (PD) patients as measured by voiding diaries.
| Number of micturations per 24 hours | Solifenacin Succinate (VESIcare) | Placebo |
|---|---|---|
| Baseline | 8.78 ± 2.18 | 9.19 ± 3.46 |
| Endpoint (12 weeks) | 8.00 ± 3.36 | 8.94 ± 3.06 |
This scale it the mean number of urinary incontinence episodes per 24 hour period, as assessed by a 3-day bladder diary. The goal is to examine the effect of solifenacin succinate (VESIcare) on urinary incontinence severity.
| Number of incontinence episodes/24 hours | Solifenacin Succinate (VESIcare) | Placebo |
|---|---|---|
| Baseline | 1.48 ± 2.56 | 1.78 ± 1.27 |
| Endpoint (12 weeks) | 0.30 ± 0.31 | 1.61 ± 1.40 |
To examine the effect of solifenacin succinate (VESIcare) on Parkinson's disease severity. The UPDRS total score ranges from 0 (no disability) to 199 (total disability).
| units on a scale | Solifenacin Succinate (VESIcare) | Placebo |
|---|---|---|
| Baseline | 25.00 ± 9.70 | 25.67 ± 12.26 |
| Endpoint (12 weeks) | 21.67 ± 9.59 | 25.75 ± 8.76 |
This scale is used to assess quality of life in Parkinson's Disease patients. Parkinson's disease quality of life scale has a possible point range from 37 (worst outcome) to 185 (best outcome). The goal of this outcome measure is to examine the effect of solifenacin succinate (VESIcare) on quality of life.
| units on a scale | Solifenacin Succinate (VESIcare) | Placebo |
|---|---|---|
| Baseline | 125.00 ± 20.95 | 114.50 ± 10.73 |
| Endpoint (12 weeks) | 116.00 ± 26.42 | 112.92 ± 17.19 |
To examine the effect of solifenacin succinate (VESIcare) on urinary incontinence severity
| Number of nocturia episodes per 24 hours | Solifenacin Succinate (VESIcare) | Placebo |
|---|---|---|
| Baseline | 2.48 ± 1.59 | 1.92 ± 1.14 |
| Endpoint (12 weeks) | 2.04 ± 1.96 | 1.78 ± 0.88 |
Non-serious events are listed at a 5% frequency threshold.
| Group | Deaths | Serious | Other |
|---|---|---|---|
| Solifenacin Succinate (VESIcare) | — | 0/10 (0%) | 4/10 (40%) |
| Placebo | — | 0/13 (0%) | 0/13 (0%) |
| Event | Solifenacin Succinate (VESIcare) | Placebo |
|---|---|---|
| XerostomiaSkin and subcutaneous tissue disorders | 2/10 | 0/13 |
| ConstipationGastrointestinal disorders | 1/10 | 0/13 |
| urinary retentionRenal and urinary disorders | 1/10 | 0/13 |
| Age, Customized(years) | Solifenacin Succinate (VESIcare) | Placebo | Total |
|---|---|---|---|
| Age (years) | 67.6 ± 6.6 | 66.5 ± 9.3 | 66.96 ± 8.04 |
| Sex: Female, Male(Participants) | Solifenacin Succinate (VESIcare) | Placebo | Total |
|---|---|---|---|
| Female | 3 | 5 | 8 |
| Male | 7 | 8 | 15 |
| Ethnicity (NIH/OMB)(Participants) | Solifenacin Succinate (VESIcare) | Placebo | Total |
|---|---|---|---|
| Hispanic or Latino | 1 | 1 | 2 |
| Not Hispanic or Latino | 9 | 12 | 21 |
| Unknown or Not Reported | 0 | 0 | 0 |
| Race (NIH/OMB)(Participants) | Solifenacin Succinate (VESIcare) | Placebo | Total |
|---|---|---|---|
| American Indian or Alaska Native | 0 | 0 | 0 |
| Asian | 0 | 0 | 0 |
| Native Hawaiian or Other Pacific Islander | 0 | 1 | 1 |
| Black or African American | 1 | 1 | 2 |
| White | 8 | 10 | 18 |
| More than one race | 0 | 0 | 0 |
| Unknown or Not Reported | 1 | 1 | 2 |
| Unified Parkinson's Disease Rating Scale (UPDRS) ADL subsection (mean)(units on a scale) | Solifenacin Succinate (VESIcare) | Placebo | Total |
|---|---|---|---|
| Mean | 9.50 ± 5.40 | 11.23 ± 4.76 | 10.48 ± 5.01 |
| Unified Parkinson's Disease Rating Scale (UPDRS) Motor subsection (Part III)(points) | Solifenacin Succinate (VESIcare) | Placebo | Total |
|---|---|---|---|
| Mean | 12.60 ± 4.38 | 14.69 ± 5.19 | 13.78 ± 4.86 |
| Unified Parkinson's Disease Rating Scale (UPDRS) Total score(units on a scale) | Solifenacin Succinate (VESIcare) | Placebo | Total |
|---|---|---|---|
| Mean | 24.00 ± 9.67 | 25.08 ± 11.93 | 24.61 ± 10.78 |
| Parkinson's Disease Quality of Life (PDQOL) total score(units on a scale) | Solifenacin Succinate (VESIcare) | Placebo | Total |
|---|---|---|---|
| Mean | 124.10 ± 19.96 | 115.31 ± 10.68 | 119.13 ± 15.65 |
7 further baseline measures are reported on the registry.
This study is completed, as verified in Nov 2021. You cannot join it, but the record below documents what was studied.
Get an email when the registry record changes — status, dates, results — or when someone posts here.
Sign in to followQuestions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.
Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.
Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.
University of South Florida